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Clinical Trials/NCT06751147
NCT06751147
Completed
Not Applicable

Effects of Lateral Femoral Cutaneous Nerve Mobilization With and Without Muscle Energy Techniques on Neuropathic Pain, Knee Range of Motion and Quality of Life in Pregnant Females

Riphah International University2 sites in 1 country48 target enrollmentDecember 23, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Meralgia Paresthetica
Sponsor
Riphah International University
Enrollment
48
Locations
2
Primary Endpoint
quality of life is assessed by QOL questioner
Status
Completed
Last Updated
9 months ago

Overview

Brief Summary

The rationale of this study is to provide empirical evidence regarding the efficacy and safety of neural mobilization in pregnant women with meralgia paresthetica. By investigating the potential benefits of this intervention, healthcare professionals can make informed decisions about incorporating neural mobilization into the management of this condition during pregnancy. Focusing on the impact of neural mobilization and muscle energy techniques on both neuropathic pain and quality of life aligns with a patient-centered approach to care. The goal is not only to reduce symptoms but also to enhance overall well-being and functional capacity

Detailed Description

The literature gap of the study is that upto our knowledge, there is little or no evidence found in previous researches on the combined effects of lateral femoral cutaneous nerve mobilization in combination with MET in pregnant females. Secondly no quantitative measurement as range of motion with goniometer has been yet studied

Registry
clinicaltrials.gov
Start Date
December 23, 2024
End Date
May 15, 2025
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ranges from 18 to 40 years
  • Body mass index ≥25kg/m
  • Pregnant females in third trimester diagnosed with myalgia paraesthetica.
  • Multigravida pregnant females
  • Patients will be screened through Prone Knee Bend (PKB) test for femoral nerve compression.
  • Positive pelvic compression test(1)

Exclusion Criteria

  • Those having other entrapment syndromes or radicular symptoms
  • Motor weakness
  • Having a history or ongoing cancerous proliferation
  • Active infection

Outcomes

Primary Outcomes

quality of life is assessed by QOL questioner

Time Frame: at base line pre intervention, at the end of 4th week post intervention

EQ-5D is used to measure quality of life

Knee range of motion is used to measure ROM

Time Frame: at base line pre intervention, at the end of 4th week post intervention

measured by goniometer

neuropathic pain

Time Frame: at base line pre intervention, at the end of 4th week post intervention

The Neuropathic Pain Scale (NPS) is a tool used to assess the specific qualities of pain associated with neuropathic pain. It helps differentiate neuropathic pain from other types of pain by evaluating different pain sensations and their intensity. The NPS consists of 10 items, each rated on a scale of 0 to 10, where 0 is "no pain" and 10 is the "worst imaginable pain".

Study Sites (2)

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