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CompletedNCT04747119METUpdated Feb 10, 2021

Effect of MET on Meralgia Paraesthesia Postpartum "Muscle Energy Technique"

An interventional study of muscle energy technique and conventional selected physical therapy in Meralgia Paresthetica and Femoral Neuropathy, sponsored by October 6 University. Completed at 1 site in Egypt. Open to female participants aged 25 Years to 40 Years. Per ClinicalTrials.gov, last updated 2021-02-10.

Sponsored by October 6 University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
25 Years to 40 Years
Sex
Female
01

Study summary

To investigate the effect of muscle energy technique on Femoral meralgia paraesthesia in a postpartum female. BACKGROUND: meralgia paraesthesia is one of the serious disorders in the postpartum female which results in pain and less physical activities.

.........HYPOTHESES:

This study hypothesized that:

muscle energy technique will have a significant effect on Femoral meralgia paraesthesia in postpartum female

Read the detailed description

Thirty meralgia paraesthesia postpartum females will participate in this study.

The patients will randomly be divided into two equal groups; the control group received the conventional selected exercise program and the study group received the same exercise training program in addition to muscle energy technique, three times per week for four weeks.

The evaluation methods by Femoral nerve conduction velocity will be measured via the Neuropack S1 MEB9004 EMG device before the exercise program and after finishing the exercise program, and also the Pelvic compression test and Pain numeric rating scale

02

Conditions studied

  • Meralgia Paresthetica
  • Femoral Neuropathy

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03

Who can participate

Ages eligible
25 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Thirty meralgia paraesthesia postpartum female Patients
  • with positive Pelvic compression test
  • age ranging from 25:40 years
  • post vaginal delivery or post-operative (postpartum) persistent dysthesia in anterolateral thigh (one side or both)
  • body mass index (20:29.9) Kg/m2

Exclusion criteria

Exclusion Criteria:

  • difficulty to communicate or to understand program instructions
  • other conditions that caused pain (for example fibromyalgia and arthritis)
  • any psychiatric or cognitive symptoms any other musculoskeletal disorders or neurologic diseases of the lower extremities and spine
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    study group

    received the conventional selected exercise program in addition to muscle energy technique

    Other: muscle energy technique · Other: conventional selected physical therapy

  • Experimental
    control group

    received the conventional selected exercise program

    Other: conventional selected physical therapy

Interventions

  • Othermuscle energy technique

    the patient was supine and the therapist fix the lower limb of the affected side then ask the patient to perform isometric contraction for abductors maintained for 3-5 seconds, then the patient was instructed to stop, exhale and relax then the therapist perform further adducted the patient's knee of the affected side as a stretching exercise for Three to five repetitions of these directions were performed.

  • Otherconventional selected physical therapy

    1. life style modification 2. Transcutaneous electrical nerve stimulation (TENS) 3. Flexibility stretching exercises to the hip flexors

05

What researchers measure

Primary outcomes

  1. Femoral nerve conduction latency

    Femoral nerve conduction latency measured via the Neuropack S1 MEB9004 EMG device

    Time frame: 4 weeks

Secondary outcomes

  1. Pelvic compression test

    the therapist applied a downward compression force to the pelvis and maintained a pressure for 45 seconds. If the patients reported an alleviation of symptoms the test is considered positive

    Time frame: four weeks

  2. Numeric Pain Rating Scale (NPRS)

    it includes 11-point numeric scale ranges from no pain with score of "0" to worst pain imaginable with score of "10"

    Time frame: four weeks

06

Study locations

1 site
  • Lama S Mahmoud
    Al Jīzah, Select State, Egypt
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT04747119
Lead sponsor
October 6 University
Responsible party
Lama Saad El-Din Mahmoud (Lecturer of physical therapy, Department of Neuromuscular disorders and its surgery, faculty of physical therapy, october 6 univerisity, October 6 University) — Principal investigator
First posted
Feb 10, 2021
Start date
Oct 1, 2020
Primary completion
Dec 30, 2020
Completion
Jan 30, 2021
Last update
Feb 10, 2021

Study contacts

Lama Saad Mahmoud, PHD
study chair · October 6 University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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