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Clinical Trials in Egypt / NCT07855380
Recruiting Not applicable

Ultrasound Guided- Chemical Rectus Sheath Block for Chronic Pain After Abdominal Midline Incision in Cancer Surgeries

NCT07855380 · tracked via the Priya Life Science Egypt tracker
Sponsor
National Cancer Institute, Egypt
Phase
Not applicable
Started
2026-05-01
Last updated
2026-10-02

Condition(s) studied

Chemical Rectus Sheath BlockChronic PainAbdominal Midline IncisionCancer Surgeries

Investigational drug(s) / intervention(s)

Saline 0.9%Transversalis fascia plane block →

Saline 0.9%: Patients will receive a sham block was performed using an equivalent volume of normal saline 0.9%.

Transversalis fascia plane block: Patients will receive ultrasound guided transversalis fascia plane block.

Study summary

The aim of this study is to evaluate peri-operative analgesia efficacy of ultrasound guided transversalis fascia plane block in cancer patients undergoing inguinal lymph node dissection

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * American Society of Anesthesiologists (ASA) class I and II. * Age ≥ 18 and ≤ 65 Years. * Cancer patients for inguinal lymph node dissection. * Body mass index (BMI): \> 20 kg/m2 and \< 40 kg/m2. Exclusion Criteria: * Patient refusal. * Local infection at the puncture site. * Coagulopathies with platelet count below 50,000 or an INR\>1.6. * Unstable cardiovascular disease. * History of psychiatric and cognitive disorders. * Patients allergic to medication used.

Primary outcome measure(s)

  • Degree of pain — 24 hours postoperatively
    Each patient will be instructed about postoperative pain assessment with the numeric rating scale (NRS) score. NRS (0 represents "no pain" while 10 represents "the worst pain imaginable").

Trial sites (1)

FacilityCityRegionStatus
Cairo University Cairo Egypt Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07855380 on ClinicalTrials.gov ↗ ← All trials in Egypt