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Postoperative Analgesia clinical trials

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NCT ID: NCT04690894 Completed - Clinical trials for Postoperative Analgesia

Erector Spinae Muscle Block Versus Caudal Block by Sonar in Pediatrics Undergoing Lower Abdominal Surgery

Start date: July 15, 2019
Phase: N/A
Study type: Interventional

this prospective randomized double blind controlled study was conducted on 60 child scheduled for lower abdominal surgery under general anesthesia. the patients were randomly allocated into 3 parallel groups.group (ESB) patients received ultrasound-guided erector spinae block in a dose of 0.4mg/ml of 0.25%bupivacaine between the 10th transverse process and erector spinae muscles.group(CB) patients received ultrasound-guided caudal block in a dose of 2.5mg/kg of 0.25%bupivacaine. group(CO) did,t received any block

NCT ID: NCT04689633 Completed - Clinical trials for Postoperative Analgesia

Quadratus Lumborum Block Versus Erector Spinae Block in Laparoscopic Cholecystectomy

Start date: April 15, 2019
Phase: N/A
Study type: Interventional

The patients were randomly allocated into 3 parallel groups of 20 patients in each group by using computer generated tables. group(Q):received bilateral sonar-guided quadratus lumborum bolck using 20 ml bupivacaine 0.25%on each side.group(E): received bilateral ultrasound-guided erector spinae block using 20 ml bupivaciane 0.25%on each side. group(C):didn't received any block

NCT ID: NCT04579302 Completed - Clinical trials for Postoperative Analgesia

Serratus Anterior Block and Erector Spinae Block in Postoperative Analgesia

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

90 patients scheduled for thoracic cancer surgeries, allocated in 3 groups for serratus anterior block and erector spinae block and control group. during anaesthesia:total intraoperative fentanyl required will be recorded. After surgery, all patients will be connected to PCA device containing morphine solution, the amount of morphine consumed during the first 24 hours will be recorded.

NCT ID: NCT04483323 Completed - Clinical trials for Postoperative Analgesia

Erector Spinae Plane Block Versus Intraarticular Injection for Postoperative Analgesia in Shoulder Arthroscopy

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

To improve the outcome after surgery, effective pain control is needed. The aim of the current study was to compare the efficacy of ultrasound guided erector spinae plane block versus the intra articular injection of local anesthetic for post-operative analgesia in patients undergoing shoulder arthroscopy.

NCT ID: NCT04374318 Completed - Clinical trials for Postoperative Analgesia

Comparison Between Intrathecal and Intravenous Dexmedetomidine

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

A prospective, randomized, comparative controlled clinical trial, aiming to compare the use of intrathecal dexmedetomidine by intravenous dexmedetomidine in concern of the first request to analgesia. The secondary end-points were the total postoperative analgesic consumption as well as the VAS.

NCT ID: NCT04336917 Completed - Clinical trials for Postoperative Analgesia

Ultrasound Guided Rhomboid Intercostal and Subserratus Plane Block in Breast Cancer Surgeries

Start date: August 31, 2020
Phase: Phase 4
Study type: Interventional

Postoperative analgesia after breast cancer surgery is a challenge for anesthesiologists due to the complex innervation of the breast. Interfascial plane blocks of the chest are gaining widespread popularity with the introduction of ultrasonography into the regional anesthesia practice. We aimed to investigate the efficacy of Rhomboid intercostal and subserratus plane block (RISS) for postoperative analgesia in patients undergoing breast cancer surgery.

NCT ID: NCT04111848 Completed - Clinical trials for Postoperative Analgesia

Magnesium and Ketamine in Postoperative Analgesia

Start date: November 1, 2019
Phase: Phase 4
Study type: Interventional

90 female patients scheduled for cancer breast surgeries will be assigned to 2 groups, each of 45. Group (K) will receive a bolus of 0.5 mg/kg ketamine with induction of anaesthesia, followed by ketamine infusion 0.12 mg/kg/hour continued till 24 hours after surgery. Group (KM) will receive a bolus of 0.5 mg/kg ketamine added to 50mg/kg magnesium sulfate over 30 minutes after induction of anaesthesia, followed by ketamine infusion 0.12 mg/kg/hour added to 8mg/kg/hour of magnesium sulfate continued till 24 hours after surgery. The same anaesthetic regimen will be applied to all patients. Total intraoperative fentanyl required to maintain mean blood pressure within 20% of its baseline will be recorded. After surgery, all patients will be connected to PCA device containing morphine solution, the amount of morphine consumed during the first 24 hours will be recorded. In the follow-up visits after 3 months, all patients will be assessed for neuropathic pain by DN4 questionnaire.

NCT ID: NCT03940469 Completed - Clinical trials for Postoperative Complications

Dexmedetomidine Versus Dexamethasone With Levobupivacaine in Interscalene Block

IBBB
Start date: July 3, 2016
Phase: Phase 4
Study type: Interventional

The investigators compared between dexamethasone and dexmedetomidine when added to levobupivacaine in the quality and duration of ultrasound-guided interscalene block during shoulder arthroscopy.

NCT ID: NCT03885427 Completed - Clinical trials for Postoperative Analgesia

Analgo-Sedative Effects Of Oral, Or Nebulized Ketamine In Pre-schoolers Undergoing Elective Surgery.

Start date: March 27, 2019
Phase: Early Phase 1
Study type: Interventional

the primary objective of this study is to investigate the sedative, and analgesic effects of oral, or nebulized ketamine as premedication drugs, and providing postoperative analgesia for the preschoolers and decrease their need for systemic analgesia.The secondary objective is to compare each sedation technique after oral, or nebulized ketamine for safety ,and procedural outcomes.

NCT ID: NCT03863977 Completed - Clinical trials for Postoperative Analgesia

Post-operative Analgesic Effects of Dexamethasone Added to Bupivacaine in Transversusabdominis Plane (TAP) Block

Start date: March 15, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

To compare the postoperative analgesic effect of two doses of dexamethasone added to bupivacaine in ultrasound-guided TAP block for inguinal hernia repair.