Devices and related methods for targeted pressure and temperature therapies for pelvic region disorders and syndromes

1. A method for the relief of pelvic region symptoms relating to diseases, disorders, syndromes and conditions of the pelvic region by targeted internal therapy, said method comprising the steps of:

locating one or more intra-rectal or intra-vaginal treatment points within the vaginal or rectal cavity of a human subject, said treatment points being selected from the group consisting of locations of muscle spasms, trigger points and sites of said symptoms;

providing a handheld device comprising a body portion having two ends, said handheld device being integrally formed from a nonporous material capable of holding temperature and transmitting heat or cold energy to tissue, a first end of said device ends terminating in a generally bulbous tip;

treating said device to raise or lower the temperature of the device;

inserting one of said device ends into the subject's rectal or vaginal cavity and thereby bringing the inserted end into contact with one of the treatment points;

maintaining contact with the treatment point to cause a therapeutic response to occur; and

applying pressure to said treatment point in contact with said inserted end, wherein the applying pressure step is performed for approximately 30 seconds to approximately 90 seconds.

2. The method according to claim 1 , wherein said generally bulbous tip has a diameter greater than a diameter of said body portion.

3. The method according to claim 2 , wherein said generally bulbous tip comprises a semi-sphere.

4. The method according to claim 1 , wherein said therapeutic response includes a trigger point release response, a pain relief occurs, a discomfort relief response, or an inflammation abating response.

5. The method according to claim 1 , wherein the relief response comprises softening of the treatment point.

6. The method according to claim 1 , further comprising:

repositioning the handheld device;

bringing the inserted end into contact with another of the treatment points; and

repeating said maintaining contact with the treatment point step.

7. The method according to claim 1 , wherein said device is used internally for approximately 8-10 minutes.

8. The method according to claim 1 , wherein said device is used internally until it returns to room or body temperature.

9. The method according to claim 1 , wherein said treating of said device comprises heating the device to a temperature above body temperature and below approximately 105° F.

10. The method according to claim 1 , wherein said treating of said device comprises heating the device to a temperature below room temperature and above approximately 45° F.

11. The method according to claim 1 , wherein the bulbous tip of the handheld device has a diameter that is approximately 1.5 to 2 times the diameter of said body portion.

12. The method according to claim 11 , wherein the bulbous tip of the handheld device has a diameter of approximately 27.5 mm.

13. The method according to claim 1 , wherein the handheld device is integrally formed from medical grade glass.

14. The method according to claim 13 , wherein said medical grade glass is Type 1 borosilicate.

15. The method according to claim 1 , wherein said symptoms are selected from the group consisting of pain, discomfort, soreness, weakness, inflammation, pressure, muscle spasms, itching, burning and irritation.

16. A method for the relief of pelvic region symptoms relating to diseases, disorders, syndromes and conditions of the pelvic region by targeted internal therapy, said method comprising the steps of:

locating one or more intra-rectal or intra-vaginal treatment points within the vaginal or rectal cavity of a human subject, said treatment points being selected from the group consisting of locations of muscle spasms, trigger points and sites of said symptoms;

providing a handheld device comprising a body portion having two ends, said handheld device being integrally formed from a nonporous material capable of holding temperature and transmitting heat or cold energy to tissue, a first end of said device ends terminating in a generally bulbous tip;

treating said device to raise or lower the temperature of the device;

inserting one of said device ends into the subject's rectal or vaginal cavity and thereby bringing the inserted end into contact with one of the treatment points;

maintaining contact with the treatment point to cause a therapeutic response to occur;

and applying pressure to said treatment point in contact with said inserted end, wherein said applying of pressure comprises delivering pressure at said treatment site at or below a moderate discomfort level for the patient, wherein said moderate discomfort level is defined as below a point at which the patient winces or tenses involuntarily.

17. A method for the relief of pelvic region symptoms relating to diseases, disorders, syndromes and conditions of the pelvic region by targeted internal therapy, said method comprising the steps of:

locating one or more intra-rectal or intra-vaginal treatment points within the vaginal or rectal cavity of a human subject, said treatment points being selected from the group consisting of locations of muscle spasms, trigger points and sites of said symptoms;

providing a handheld device comprising a body portion having two ends, said handheld device being integrally formed from a nonporous material capable of holding temperature and transmitting heat or cold energy to tissue, a first end of said device ends terminating in a generally bulbous tip;

treating said device to raise or lower the temperature of the device;

inserting one of said device ends into the subject's rectal or vaginal cavity and thereby bringing the inserted end into contact with one of the treatment points;

maintaining contact with the treatment point to cause a therapeutic response to occur; and

applying pressure to said treatment point in contact with said inserted end, wherein the applying pressure step comprises applying pressure at a plurality of dissimilar angles to the treatment point.

18. A method for the relief of pelvic region symptoms relating to diseases, disorders, syndromes and conditions of the pelvic region by targeted internal therapy, said method comprising the steps of:

locating one or more intra-rectal or intra-vaginal treatment points within the vaginal or rectal cavity of a human subject, said treatment points being selected from the group consisting of locations of muscle spasms, trigger points and sites of said symptoms;

providing a handheld device comprising a body portion having two ends, said handheld device being integrally formed from a nonporous material capable of holding temperature and transmitting heat or cold energy to tissue, a first end of said device ends terminating in a generally bulbous tip;

treating said device to raise or lower the temperature of the device;

inserting one of said device ends into the subject's rectal or vaginal cavity and thereby bringing the inserted end into contact with one of the treatment points;

and maintaining contact with the treatment point to cause a therapeutic response to occur; and

wherein the body portion of the handheld device has at least two bends such that said device adopts an S-shaped or lightning bolt shape in profile.

19. A method for the relief of pelvic region symptoms relating to diseases, disorders, syndromes and conditions of the pelvic region by targeted internal therapy, said method comprising the steps of:

locating one or more intra-rectal or intra-vaginal treatment points within the vaginal or rectal cavity of a human subject, said treatment points being selected from the group consisting of locations of muscle spasms, trigger points and sites of said symptoms;

providing a handheld device comprising a body portion having two ends, said handheld device being integrally formed from a nonporous material capable of holding temperature and transmitting heat or cold energy to tissue, a first end of said device ends terminating in a generally bulbous tip;

treating said device to raise or lower the temperature of the device;

inserting one of said device ends into the subject's rectal or vaginal cavity and thereby bringing the inserted end into contact with one of the treatment points;

and maintaining contact with the treatment point to cause a therapeutic response to occur; and wherein said patient has been diagnosed with an inflammatory, non-infectious pain syndrome selected from the group consisting of pelvic floor dysfunction, dyspareunia, vaginismus, non-bacterial prostatitis, vulvodynia and interstitial cystitis.

20. The method according to claim 19 , wherein the handheld device is integrally formed from medical grade glass.

21. The method according to claim 20 , wherein said medical grade glass is Type 1 borosilicate.

22. The method according to claim 19 , wherein said generally bulbous tip has a diameter greater than a diameter of said body portion.

23. The method according to claim 22 , wherein said generally bulbous tip comprises a semi-sphere.

24. A method for the relief of pelvic region symptoms relating to interstitial cystitis by targeted internal therapy, said method comprising the steps of:

locating one or more intra-rectal or intra-vaginal treatment points within the vaginal or rectal cavity of a human subject, said treatment points being selected from the group consisting of locations of muscle spasms, trigger points and sites of said symptoms;

providing a handheld device comprising a body portion having two ends, said handheld device being integrally formed from a nonporous material capable of holding temperature and transmitting heat or cold energy to tissue, a first end of said device ends terminating in a generally bulbous tip and the body portion of the handheld device having at least two bends such that said device adopts an S-shaped or lightning bolt shape in profile;

treating said device to raise or lower the temperature of the device;

inserting one of said device ends into the subjects rectal or vaginal cavity and thereby bringing the inserted end into contact with one of the treatment points;

and maintaining contact with the treatment point to cause a therapeutic response to occur.

25. The method according to claim 24 , wherein the handheld device is integrally formed from medical grade glass.

26. The method according to claim 25 , wherein said medical grade glass is Type 1 borosilicate.

27. The method according to claim 24 , wherein said generally bulbous tip has a diameter greater than a diameter of said body portion.

28. The method according to claim 27 , wherein said generally bulbous tip comprises a semi-sphere.

29. The method according to claim 24 , wherein the bulbous tip of the handheld device has a diameter that is approximately 1.5 to 2 times the diameter of said body portion.

30. The method according to claim 29 , wherein the bulbous tip of the handheld device has a diameter of approximately 27.5 mm.

31. The method according to claim 24 , wherein said symptoms are selected from the group consisting of pain, discomfort, soreness, weakness, inflammation, pressure, muscle spasms, itching, burning and irritation.