- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05979766
Manual Lymphatic Drainage vs Marian Clark Drainage in Pcs
Effects of Manual Lymphatic Drainage Versus Marian Clark Drainage on Pain and Disability in Patients With Pelvic Congestion Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Amjad, PhD
- Phone Number: 03324390125
- Email: Imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Recruiting
- Jinnah Hospital
-
Contact:
- Hafiza Neelam Muneeb, PT
- Phone Number: +92 320 4097476
- Email: hafiza.neelam@riphah.edu.pk
-
Principal Investigator:
- Maira Imran Butt, MS-WHPT
-
Sub-Investigator:
- Hafiza Neelam Muneeb
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Multiparous women
- Age ranging 20 to 50
- Ovarian veins >4mm in diameter on Ultrasound Chronic pelvic pain/pressure for more than 6 months.
- Dull, aching or "dragging" pain in the pelvis or lower back, particularly on standing and worse around the time of your menstrual period.
- Pelvic pain that worsens as the day goes on, particularly if much time is spent standing dyspareunia
- Swollen veins in pelvic region, butt, thighs, vulva and vagina.
- Associated Irritable bladder/Irritable bowel present
Exclusion Criteria:
- Pelvic pain due to other organic cause like uterine fibroids, Endometriosis, Ovarian cyst pelvic pain due to neurological or musculoskeletal disorder
- Uterine prolapse
- Pelvic cancer
Study Plan
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 |
|---|---|
|
Active Comparator: Manual lymphatic drainage vs marian clark drainage
Effect of Marian Clark drainage and manual lymphatic drainage in women suffering from pelvic congestion syndrome
|
Manual lymphatic drainage versus marian clark drainage
|
|
Active Comparator: Manual lymphatic drainage versus marian clark drainage
Effect of Marian Clark drainage and manual lymphatic drainage in women suffering from pelvic congestion syndrome
|
Manual lymphatic drainage versus marian clark drainage
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Manual lymphatic drainage
Time Frame: 6 months
|
Treatment protocol to group A It consists of 15 patients who will receive manual lymphatic drainage 4 sessions per week for 12 weeks Manual Lymph Drainage Techniques for Pelvic Decongestion Step 1: short neck treatment (supraclavicular fossa or SCF) Step 2: (two parts: visceral, deep) Visceral: Deep: Treatment of the thoracic duct, cisterna Chyli Deep Abdominal Manual lymphatic drainage Step-3. Treatment of right Axillary Lymph nodes Step-4. Establish the Right inguino-Axillary Anastomosis. Step-5. Decongest the right ipsilateral lower abdomen and suprapubic area Step-6 Treatment of Left Axillary Lymph nodes Step-7. Establish the Left inguino-Axillary Anastomosis. Step-8. Decongest the Let ipsilateral lower abdomen and suprapubic area |
6 months
|
|
Marian clark drainage
Time Frame: 6 months
|
It consists of 15 patients who will receive Marian clark drainage 4 sessions per week for 12 weeks each session will continue till therapist feels palpable change in congestion in pelvic area medial to Anterior superior Iliac spine.
|
6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hafiza Neelam Muneeb, Ms, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RiphahIUmib
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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