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CompletedNCT07729254Updated Sep 16, 2026

Association Between Cesarean Scar Mobility and Menstrual Pain in Post-Cesarean Women

An observational study in Cesarean Section and Dysmenorrhea, sponsored by Cairo University. Completed at 1 site in Egypt. Open to female participants aged 20 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-09-16.

Sponsored by Cairo University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
51
Ages
20 Years to 35 Years
Sex
Female
01

Study summary

The aim of this observational cross-sectional study is to investigate the association between cesarean scar mobility and menstrual pain severity in women following cesarean section. The study will enroll women aged 20 to 35 years with a history of cesarean delivery who experience menstrual pain. Baseline assessments will be performed to evaluate cesarean scar mobility, menstrual pain severity, pressure pain threshold, and related clinical characteristics. The findings will help clarify whether reduced cesarean scar mobility is associated with greater menstrual pain severity and may provide evidence supporting the clinical assessment of cesarean scars in women with post-cesarean menstrual pain.

Read the detailed description

Cesarean section is one of the most frequently performed surgical procedures worldwide. Although generally safe, postoperative scar formation and fascial adhesions may result in long-term alterations in tissue mobility and biomechanics. These changes have been suggested to contribute to persistent symptoms, including menstrual pain, chronic pelvic pain, abdominal tenderness, and functional impairment. Despite increasing interest in cesarean scar assessment, the relationship between scar mobility and menstrual pain severity has not been sufficiently investigated.

Restricted scar mobility may influence the mechanical behavior of the abdominal wall and surrounding fascial structures, potentially contributing to altered force transmission, increased tissue sensitivity, and pain during menstruation. Understanding this relationship may improve the clinical evaluation of women presenting with post-cesarean menstrual pain and assist in identifying patients who may benefit from targeted rehabilitation interventions.

This observational cross-sectional study aims to investigate the association between cesarean scar mobility and menstrual pain severity in women following cesarean section. Baseline measurements will be obtained to assess cesarean scar mobility, menstrual pain severity, pressure pain threshold, and selected demographic and obstetric characteristics. Correlation and regression analyses will be performed to determine whether cesarean scar mobility is associated with menstrual pain severity and whether it independently predicts menstrual pain after controlling for potential confounding variables.

The findings of this study are expected to improve understanding of the clinical significance of cesarean scar mobility in women with menstrual pain and provide evidence to support comprehensive scar assessment as part of women's health physical therapy practice.

02

Conditions studied

  • Cesarean Section
  • Dysmenorrhea

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Keywords

  • Cesarean Scar
  • Scar Mobility
  • Dysmenorrhea
  • Menstrual Pain
  • Visual Analog Scale
  • Adheremeter
  • Pressure Pain Threshold
  • Post-Cesarean Women
03

In context

Dysmenorrhea

398 studies on the registry are indexed under Dysmenorrhea; 96 are open to participants now.

This study's enrollment of 51 is below the median of 123 across 56 observational studies indexed under Dysmenorrhea.

Browse Dysmenorrhea studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Women aged 20-35 years with a previous cesarean section who experience menstrual pain.

Inclusion criteria

  • Females aged 20-35 years.
  • History of at least one cesarean section.
  • Regular menstrual cycles.
  • Presence of menstrual pain during the previous three menstrual cycles.
  • Body mass index (BMI) between 18.5 and 29.9 kg/m².
  • Willingness to participate and provide written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Current pregnancy.
  • History of pelvic or abdominal surgery other than cesarean section.
  • Endometriosis or adenomyosis.
  • Uterine fibroids associated with pelvic pain.
  • Pelvic inflammatory disease.
  • Congenital uterine anomalies.
  • Neurological disorders affecting pain perception.
  • Current use of hormonal therapy or medications affecting pain perception.
  • Active skin infection or open wound over the cesarean scar.
  • Malignancy.
  • Inability to complete study assessments.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
51 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Menstrual Pain Severity

    Menstrual pain severity will be assessed using the 10-cm Visual Analog Scale (VAS), where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater menstrual pain severity.

    Time frame: Baseline

  2. Cesarean Scar Mobility

    Cesarean scar mobility will be assessed using the Adheremeter. Higher scores indicate

    Time frame: Baseline

Secondary outcomes

  1. Pressure Pain Threshold

    Pressure pain threshold will be measured using a pressure algometer. Higher values indicate a higher pressure pain threshold.

    Time frame: Baseline

  2. WaLIDD Score

    The severity of dysmenorrhea will also be evaluated using the Working ability, Location, Intensity, Days of pain, and Dysmenorrhea (WaLIDD) Score as a secondary clinical measure. The total score ranges from 0 to 12, with higher scores indicating more severe dysmenorrhea.

    Time frame: Baseline

07

Study locations

1 site
  • Faculty of Physical Therapy Outpatient Clinic
    Cairo, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07729254
Lead sponsor
Cairo University
Responsible party
Amira Ibrahim Hassanein Abdel-aal (Lecturer of Physical Therapy for Women's Health, Horus University) — Principal investigator
First posted
Jul 27, 2026
Start date
Jul 23, 2026
Primary completion
Aug 25, 2026
Completion
Aug 25, 2026
Last update
Sep 16, 2026

Oversight

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

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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