Manual Lymphatic Drainage vs Marian Clark Drainage in Pcs

July 31, 2023 updated by: Riphah International University

Effects of Manual Lymphatic Drainage Versus Marian Clark Drainage on Pain and Disability in Patients With Pelvic Congestion Syndrome

Pelvic congestion syndrome is a debilitating and potentially life threatening disorder of the pelvic region there is a constant hindrance in patient's daily professional and personal life due to the chronic pain. it can provide a definite way to improve pelvic congestion and quality of life. In this way it can benefit a large percentage of community females suffering from pelvic congestion syndrome and disability. This can grow at large length in favour of patients, clinicians and overall women health.

Study Overview

Detailed Description

As per researcher's knowledge there are limited researches in which efficacy of manual lymphatic drainage in pelvic congestion syndrome are analyzed furthermore my comparative intervention i.e Marian Clark drainage is a rarely used osteopathic technique and not much studies have been conducted on it. This study helped to in identifying the effect of manual lymphatic drainage versus Marian Clark drainage on pain and disability in patients with pelvic congestion syndrome.

Study Type

Interventional

Enrollment (Estimated)

26

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 Contact

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan
        • Recruiting
        • Jinnah Hospital
        • Contact:
        • Principal Investigator:
          • Maira Imran Butt, MS-WHPT
        • Sub-Investigator:
          • Hafiza Neelam Muneeb

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:

  • 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

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
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.

  • Stand to the side of the patient
  • Patient semiprone on all fours
  • Hook fingers medial to both Anterior superior Iliac spine
  • Pull hands cephalad (traction)
  • Patient arches back like a cat
  • Encourage this movement with cephalad rocking
  • Repeat for several minutes
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hafiza Neelam Muneeb, 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 5, 2022

Primary Completion (Estimated)

August 1, 2023

Study Completion (Estimated)

August 1, 2023

Study Registration Dates

First Submitted

July 31, 2023

First Submitted That Met QC Criteria

July 31, 2023

First Posted (Actual)

August 7, 2023

Study Record Updates

Last Update Posted (Actual)

August 7, 2023

Last Update Submitted That Met QC Criteria

July 31, 2023

Last Verified

July 1, 2023

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)?

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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