- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06845670
Effects of Wurn Technique on Dyspareunia, Menstrual Cramps & QoL in Infertile Women
February 20, 2025 updated by: Riphah International University
Effects of Wurn Technique on Symptoms of Dyspareunia, Menstrual Cramps and Quality of Life in Women With Infertility
Wurn technique is a PT technique.
It is site specific massage therapy in the form of relaxing technique, helps to promote the function of abdominopelvic and reproductive organs.
Study Overview
Detailed Description
This study will be randomized controlled trial, will be completed in 10 months duration.
Non probability Conveninence sampling technique will be used with 54 participants after randomization.
Effect will be obseved in 2 groups.
Study Type
Interventional
Enrollment (Actual)
54
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Lahore, Pakistan
- Riphah International University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Women with infertility between age 25 to 45
- women who were unable to conceive for 12months with regular unprotected intercourse
- women with infertility indicating sexual pain, irregular periods with menstrual cramps.
- women with secondary infertility
Exclusion Criteria:
- Women with active infections and abnormal ovarian cysts.
- Any abdominopelvic surgery within last 90days.
- Any medical history of active abdominopelvic cancer or malignancy.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
Wurn technique
|
Wurn technique is a massage technique and PF relaxation exercises are to relax tighten pelvic floor muscles.
Other Names:
|
|
Experimental: Controlled group
Pelvic floor relaxation
|
Wurn technique is a massage technique and PF relaxation exercises are to relax tighten pelvic floor muscles.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Female Sexual Function Index Scoring
Time Frame: 2weeks duration
|
Measure sexual functioning of women in six domains: desire, arousal, lubrication, orgasm, satisfaction and pain
|
2weeks duration
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|
Mankoski Pain Scale
Time Frame: 2weeks duration
|
Numerical pain scale ranging from 0 to 10
|
2weeks duration
|
|
FertiQoL
Time Frame: 2weeks duration
|
Asses quality of life of an individual with infertility
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2weeks duration
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Adeela Arif, MS, Riphah International University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 26, 2023
Primary Completion (Actual)
October 26, 2024
Study Completion (Actual)
December 30, 2024
Study Registration Dates
First Submitted
February 20, 2025
First Submitted That Met QC Criteria
February 20, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 20, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Genital Diseases
- Pain
- Neurologic Manifestations
- Mental Disorders
- Pathologic Processes
- Genital Diseases, Male
- Male Urogenital Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Genital Diseases, Female
- Sexual Dysfunction, Physiological
- Sexual Dysfunctions, Psychological
- Pelvic Pain
- Menstruation Disturbances
- Infertility
- Infertility, Female
- Dyspareunia
- Dysmenorrhea
Other Study ID Numbers
- Maha Ashfaq
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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