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Postoperative Recovery clinical trials

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NCT ID: NCT04304274 Completed - Analgesia Clinical Trials

Programmed Intermittent Bolus Infusion of Thoracic Paravertebral Block for Hepatectomy

Start date: March 10, 2020
Phase: N/A
Study type: Interventional

Hepatectomy induces moderate to severe postoperative pain. Patient-controlled intravenous analgesia has been used in many medical centers for post-hepatectomy analgesia, but the effects are limited and often cause undesirable adverse effects. Regional Block has been used for postoperative analgesia in many surgeries. Some studies suggest that regional analgesia has an opioid-sparing effect and can reduce the incidence of chronic pain. Also, the programmed intermittent bolus infusion is better than continuous infusion, with less analgesic consumption and fewer adverse effects. Studies on the early and late postoperative analgesia and recovery effects of paravertebral block for open hepatectomy are scarce. Therefore, the investigators aim to conduct a prospective, randomized, subject and assessor-blinded, parallel-group, placebo-controlled study to test the hypothesis that the programmed intermittent bolus infusion of right thoracic paravertebral block reduces postoperative intravenous analgesic use and pain scores and improved patients' satisfaction.

NCT ID: NCT04112394 Completed - Clinical trials for Postoperative Recovery

Does Erector Spinal Block Improve Quality of Recovery After Laparoscopic Cholecystectomy

Start date: September 29, 2019
Phase: N/A
Study type: Interventional

The primary aim of this prospective, randomized study is to evaluate the effect of erector spinae block (ESP) on quality of recovery with the QoR-40 questionnaire in patients undergoing elective laparoscopic cholecystectomy.

NCT ID: NCT03981419 Completed - Clinical trials for Postoperative Recovery

A Study to Evaluate the Effect of GRF6021 on Postoperative Recovery Following Primary Hip or Knee Arthroplasty

Start date: July 12, 2019
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety, tolerability and effect of GRF6021 on clinical recovery parameters in participants undergoing primary hip or knee arthroplasty.

NCT ID: NCT03955419 Completed - Clinical trials for Postoperative Recovery

Preoperative Oral Carbohydrate Loading in Gynecologic Surgery

Start date: July 25, 2019
Phase: N/A
Study type: Interventional

The advantage of carbohydrate loading in minimally invasive surgeries are not well established. We designed this study to evaluate whether preoperative oral carbohydrate improve postoperative recovery after laparoscopic gynecologic surgeries.

NCT ID: NCT03420937 Completed - Clinical trials for Postoperative Recovery

Deep Neuromuscular Block During General Anaesthesia in Robotic Surgery

Start date: June 2016
Phase: Phase 4
Study type: Interventional

The aim of this project is to show, whether the use of the deep neuromuscular block in certain laparoscopic robot-assisted surgery can positively influence main physiological functions compared to the use of standard neuromuscular block. Secondary outcome is to find out whether the targeted specific reversal of neuromuscular block by sugammadex improves and fastens the post-operative recovery of the patients.

NCT ID: NCT03350334 Completed - Postoperative Pain Clinical Trials

Perioperative Duloxetine for Pain Management After Laparoscopic Hysterectomy

Start date: December 4, 2017
Phase: N/A
Study type: Interventional

The aim of the investigators of the study is to evaluate the effect of peri-operative duloxetine on post-operative recovery in patients undergoing laparoscopic hysterectomy.

NCT ID: NCT02921529 Completed - Clinical trials for Postoperative Recovery

TEAS Enhanced Recovery After Laparoscopic Colon Surgery

ARCO
Start date: November 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to observe the effects of transcutaneous electrical acupoint stimulation(TEAS) on postoperative recovery after laparoscopic colon surgery.

NCT ID: NCT02141412 Completed - Clinical trials for Postoperative Recovery

Intravenous Dexmedetomidine For The Quaity Of Emergence From General Anesthesia

Start date: September 2009
Phase: Phase 4
Study type: Interventional

In a prospective randomized clinical trial involving adult patients undergoing elective surgery under general anesthesia, the investigators will enroll 216 patients, and evaluate 3 doses of prophylactic dexmedetomidine as a means to reduce postoperative shivering and quality of emergence from anesthesia versus placebo.