Overview
Ultrasound Guided Rectus Sheath Block and Transversus Abdominis Plane Block
Status:
Completed
Completed
Trial end date:
2023-01-02
2023-01-02
Target enrollment:
0
0
Participant gender:
All
All
Summary
The current study aimed to assess the efficacy of Dexmedetomidine (DEX) and Dexamethasone as an adjuvant to ultrasound guided TAP and RS block to prolongation of postoperative analgesia and better pain control in children undergoing laparoscopic surgeriesPhase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Assiut UniversityTreatments:
Bupivacaine
Dexamethasone
Dexmedetomidine
Criteria
Inclusion Criteria:- ● Age: 8-12years.
- Weight: 20-60 kg.
- Sex: both males and females.
- ASA physical status: I-II.
Exclusion Criteria:
- • Patient's guardian refusal to participate in the study.
- Patients having known hypersensitivity to dexametomidine will be excluded.
- Patients with cardiovascular, liver or renal disease, unsatisfactory preoperative
peripheral arterial oxygen saturation, neurological or psychiatric disease and
coagulation disturbances.
- Any perioperative cardiovascular or respiratory event occurred or difficulties in
pain perception and assessment which make the study intervention clinically
unacceptable.
- Patients on regular use of analgesic or who received analgesic 24 h before
surgery