Ultrasound Guided Erectror Spinae Block Versus Intracavitary During Medical Thoracoscopy
Starting soon · Phase 2/Phase 3
Conditions studied: PLEURA DISEASE
In brief
The primary aim: is to compare the effect of US guided ESP block at two levels versus intracavitary blockade in medical thoracoscopy on total peri-procedural (intraoperative and post-operative 12 hours) nalbuphine consumption (mg) during medical thoracoscopy. Secondary aims: Time to first rescue analgesia, postoperative VAS, haemodynamics, recovery time (Aldert \> 9), and adverse events
Key facts
- Study ID
- NCT07572019
- Run by
- Kafrelsheikh University
- People needed
- 100
- Starts
- 2026-05-15
- Expected to finish
- 2026-07-20
- Last updated by the study team
- 2026-05-12
Who can join
Age: 25 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 100 patients belonging to American Society of Anesthesiologists (ASA) I-III scheduled for medical thoracoscopy under adequate sedation and analgesia.
You may not qualify if…
- Patients will be excluded if; history of allergy or contraindication to any of the studied drugs, BMI more than 35 kg/m2 chronic opioid use or abuse, patients for whom ESPB block is contraindicated (patient refusal, coagulation disorder, skin infection at the injection site), history of post-thoracotomy, chest wall deformity, severe uncontrolled comorbidity, intubated patients, or if the interventional physician wants general anaesthesia from the start
Full record on ClinicalTrials.gov
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