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Taking people in PolandNo phase

Tests visceral therapy in women with prolapse or endometriosis pain

Tests visceral therapy against placebo in women with genital prolapse or endometriosis.

Plain-language title generated from the registry record
Registry title: Functional Links Between the Temporomandibular Joint and the Pelvis in Gynecology

Key facts

Where
Poznan, PolandSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 60 years old?

Source: NCT05978414, who can take part

Where in Poland

  • Poznan University of Physical EducationPoznan, PolandTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Poznan University of Physical Education
Trial code
NCT05978414
Record updated
24 September 2026
Original description
1 Recruitment. 2. Collection of written consents for the study. 3. Random assignment to groups with and without intervention. 4. Completion of questionnaires by study participants, postural pattern assessment, temporomandibular joint assessment, and platform assessment.Read full original descriptionShow less

Functional Relationships Between the Temporomandibular Joint and the Pelvis in Women With Gynecological Diseases of Genital Prolapse and Endometriosis

1 Recruitment. 2. Collection of written consents for the study. 3. Random assignment to groups with and without intervention. 4. Completion of questionnaires by study participants, postural pattern assessment, temporomandibular joint assessment, and platform assessment.

5. Performance of visceral therapy in the group with intervention, in the group without intervention placebo. Duration 5 weeks, treatment 1x per week at the same time of day and given day e.g. Mondays only.

6. Reassessment as in step 4. 7. Data collection, statistical analyses. 8. Interpretation of results for female participants. 9. Preparation of results for scientific publications.

Inclusion: Written consent to participate in the study; Female patients after surgical treatment with prolapse of reproductive organs and diagnosed endometriosis.

Exclusion: Cancer; Rheumatic diseases; No written consent to participate in the study; Injury to the temporomandibular joint and pelvis; Fibromyalgia; At each stage of the experiment if the patient decides that she does not want to participate she is excluded.

ClinicalTrials.gov NCT05978414