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NCT06339983
Effects of Scar Mobilization Versus Myofascial Cupping Technique on Cesarean Scar
NA trial testing Manual Scar Mobilization Therapy: in Cesarean Section; Complications, Wound, Hematoma in 30 participants. Completed in 5 October 2024.
20 September 2024
Quick facts
| Lead sponsor | Riphah International University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 1 April 2024 |
| Primary completion | 20 September 2024 |
| Estimated completion | 5 October 2024 |
| Sites | 1 location across Pakistan |
Drugs / interventions tested
- Manual Scar Mobilization Therapy:
- Myofascial Cupping Therapy:
Conditions studied
- Cesarean Section; Complications, Wound, Hematoma — all drugs for Cesarean Section; Complications, Wound, Hematoma →
Sponsor
Riphah International University
Who can join
Adults 20 to 40, female only, with Cesarean Section; Complications, Wound, Hematoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Study focuses on comparing the effects of manual scar mobilization and myofascial cupping techniques on the outcomes of pain, physical characteristics, and appearance of cesarean scars. The study aims to contribute valuable insights into tailored interventions for improving cesarean scars. The randomized clinical trial will involve 52 participants, primigravida women aged 20 to 40 with completely healed but painful cesarean scars. Excluding those with previous scar therapy or infectious scars, the participants will be divided into two groups, with Group A receiving manual scar mobilization therapy and Group B receiving myofascial cupping therapy, both administered twice a week for four weeks. Pain assessment will be conducted using a numeric pain rating scale (NPRS), while physical characteristics and appearance will be evaluated using the Manchester Scar Scale for cesarean scars (MSS). The data collected will be analyzed using SPSS version 29.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06339983
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06339983 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Riphah International University
- Last refreshed: 20 November 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06339983.
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