Indiana_Trial 01

  • STATUS
    Recruiting
  • participants needed
    120
  • sponsor
    pfizer
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Updated on 19 February 2024
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Summary

Study Overwiew

Description

Study Type : Interventional  (Clinical Trial) Estimated Enrollment : 36 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Triple (Participant, Investigator, Outcomes Assessor) Primary Purpose: Treatment Official Title: Effects of Muscle Energy Technique Versus Aerobic Exercises on Pain and Disability in Patients With Chronic Pelvic Pain Actual Study Start Date : January 1, 2022 Estimated Primary Completion Date : July 1, 2022 Estimated Study Completion Date :July 1, 2022

Details
Condition Dental Bones, Joints, & Muscles
Age 25years - 45years
Clinical Study IdentifierNCT_ID01
Sponsorpfizer
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

women with chronic pelvic pain of >6 months' duration and the cause of their pain is unknown
CPP was located within the true pelvis (between and below the anterior iliac crests)
Average score of at least 4 out of 10 (0-10) on a numeric rating scale
moderate to severe pain on pelvic pain impact questionnaire

Exclusion Criteria

History of cancer
Pregnancy at the time of inclusion
Known pelvic pathology (eg, endometriosis, ovarian cyst, fibroid >3cm)
Intraabdominal and pelvic surgery within the last six months
chronic or recurrent gastro-intestinal disease including irritable bowel syndrome
Received any physiotherapy treatment within the previous month
Ages Eligible for Study: 25 Years to 45 Years (Adult) Sexes Eligible for
Study: Female Gender Based Eligibility: Yes Gender Eligibility
Description: Pelvic pain is more common in female Accepts Healthy
Volunteers: No
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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