Investigating the effects of a specific pain relief technique on breathing after abdominal surgery
Respiratory Effects of Rectus Sheath Block in Patients Undergoing Major Upper Abdominal Surgery.
This study is testing if a special pain relief technique can help people breathe better and feel less pain after having abdominal surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | All |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Asyut, Assiut Governorate) |
| Trial ID | NCT03725527 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-50 years undergoing elective abdominal surgery with midline incisions and having a BMI of less than 30.
Not a fit: Patients who may not benefit from this study include those with coagulation disorders, infections at the injection site, or those requiring urgent abdominal surgery.
Why it matters
Potential benefit: If successful, this approach could significantly reduce postoperative pain and improve respiratory function in patients after abdominal surgery.
How similar studies have performed: Other studies have shown promising results with similar analgesic techniques, suggesting potential benefits in postoperative pain management.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Asyut, Assiut Governorate
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.