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Quality of Life and Pain Pressure Threshold in Response to Scar Release Techniques for Chronic Transverse Abdominal Scar

Unknown statusNot applicableNCT05937217
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Postoperative scarring is one of the most common concerns among surgical patients. The incidence of abnormal scarring, i.e. keloid or hypertrophic scar formation after caesarean section (CS) is reported to be 41% .That can lead to functional limitations, pruritus, pain and cosmetic issues. so, the purpose of this study is to investigate quality of life and pain pressure threshold in response to myofascial induction and direct scar release techniques for lower transverse abdominal scar

Study details

Official title
Quality of Life and Pain Pressure Threshold in Response to Myofascial Induction Therapy and Direct Scar Release Techniques for Chronic Lower Transverse Abdominal Scar
Conditions
  • Cesarean Section Complications
Interventions
  • Other: myofascial induction and direct scar release techniques
  • Device: therapeutic ultrasound
Sponsor
Cairo University
Start date
2023-07-05
Primary completion
2023-10-01
Sex
Female
Age range
from 25 Years to 35 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Women with a well healed, old , transverse cesarean section scar (more than 6 months resulted in chronic scar pain). * Pain can be intermittent or constant at rest or with activity, and it is reported to be at least at a level of about 3/ 10 on visual analogue scale at recording sites will be marked on the C-section scar at 2.5 cm intervals (Wasserman et al., 2018). * Women identified that the pain is either located in the cesarean section scar or caused by palpation of scar and it presents since the time of surgery not prior to the cesarean section. * Their ages will range from 25-35 years old. * Their BMI will be 18.5-29.9 kg/ m². Exclusion Criteria: * Acute and subacute cesarean section. * Delayed wound healing. * History of abdominal or pelvic cancer. * Active pelvic or abdominal infection. * Skin irritation/inflammation at the site of scar. * Currently pregnant women.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05937217