Investigating the effects of a specific pain relief technique on breathing after abdominal surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the respiratory and pain-relieving effects of ultrasound-guided rectus sheath block analgesia in patients undergoing elective abdominal surgery with midline incisions. The rectus sheath block targets specific sensory nerves to alleviate somatic pain from the abdominal wall, potentially improving postoperative recovery. The study will assess how this technique influences diaphragmatic function and overall respiratory outcomes following surgery. Participants will be monitored for pain levels and respiratory function postoperatively to determine the effectiveness of this intervention.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age: 18-50 years.
* Sex: both males and females.
* BMI\< 30kg/m2.
* ASA physical status: 1, II and III.
* Elective abdominal surgery with midline incisions.

Exclusion Criteria:

* Patient refusal.
* Infection at injection site
* Coagulation disorders.
* Allergy to study medications.
* Pregnancy.
* Respiratory tract infection within the last 2 weeks.
* Urgent abdominal surgery

Where it's running

• Assiut university main hospital, ICUs
  Asyut, Assiut Governorate, Egypt Recruiting

Study contacts

• Principal investigator: Noha Y Mohamed, MD — Lecturer in anesthesia and intensive care department, faculty of medicine, Assiut university, Egypt.
• Study coordinator: Noha Y Mohamed, MD
• Email: noha.hagagy@gmail.com
• Phone: +2 01001890194

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.