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Pain, Postoperative clinical trials

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NCT ID: NCT05973045 Recruiting - Post-operative Pain Clinical Trials

Investigation of the Effect of Distention Medium Temperature on Image Quality, Hyponatremia Risk, and Post-operative Pain in Operative Hysteroscopy

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

Minimally invasive applications are seen as the gold standard in today's gynecology practice and are frequently preferred by both patients and physicians. Less pain, shorter hospital stays, and better cosmetic results brought about by minimally invasive applications further increase their preference. One of these approaches is hysteroscopic interventions. Although hysteroscopy is a well-defined method, current research has focused on further reduction of pain. One of these methods is to warm the distention media at body temperature. theTaim of this study was to examine the effect of distention medium temperature on image quality, hyponatremia risk, and post-operative pain in operative hysteroscopy.

NCT ID: NCT05971368 Recruiting - Clinical trials for Post Operative Pain, Acute

A Comparative Study Between Ultrasound Guided Thoracic Paravertebral Block VS Serrartus Anterior Muscle Block in VATS as Regard Their Effectiveness in Post-operative Analgesia

Start date: June 4, 2022
Phase: N/A
Study type: Interventional

A comparative study between ultrasound guided thoracic paravertebral block VS ultrasound guided serrartus anterior muscle block in video-assisted thoracoscopic surgeries as regard their effectiveness in post-operative analgesia

NCT ID: NCT05969509 Recruiting - Pain, Postoperative Clinical Trials

Investigation of the Effect of Progressive Relaxation Exercises on Pain and Bowel Movements in Patients Undergoing Laparoscopic Cholecystectomy

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare in health conditions. The main questions it aims to answer are: Does progressive relaxation exercises reduce pain in patients undergoing laparoscopic cholecystectomy? Does progressive relaxation exercises increase bowel movements in patients undergoing laparoscopic cholecystectomy?

NCT ID: NCT05961735 Recruiting - Pain, Postoperative Clinical Trials

Comparison of PECS II Block and Combined Serratus Anterior Plane Block to Reduce Acute Pain After Mastectomy

Start date: August 1, 2023
Phase:
Study type: Observational

In this study, PECS II block or CSAB will be applied to patients who have had a modified radical mastectomy under general anesthesia for postoperative pain relief by using 30 ml of 0.25% bupivacaine .All patients will receive tramadol with a patient-controlled analgesia device during the postoperative period. Pain, nausea-vomiting, additional analgesic and antiemetic drug requirement, within 24 hours postoperatively will be compared between groups. In this study, it was aimed to compare the efficacy of both peripheral nerve block methods in patients after mastectomy.

NCT ID: NCT05958589 Recruiting - Postoperative Pain Clinical Trials

Caudal Block for Inguinal Hernioplasty in Children

Start date: January 8, 2022
Phase: Phase 3
Study type: Interventional

This is a prospective, randomized, controlled clinical study designed to determine the effectiveness of caudal block combined with general anesthesia in providing intra- and postoperative analgesia, and its effect on hemodynamic stability and drug consumption.

NCT ID: NCT05949476 Recruiting - Clinical trials for Extraction of the Lower Third Molars

Influence of Ozone Therapy on Postoperative Pain Relief in the Surgical Treatment of Lower Third Molars: Randomized Controlled Trial

Start date: July 19, 2022
Phase: N/A
Study type: Interventional

Patients will undergo a split-mouth protocol which includes: a control group: in which the extraction of the lower third molar will be performed according to the standard protocols of the structure. A study group: in which ozone will be used in addition, in two formulations: gaseous, injected into the site of the pre- and post-surgery operation, and topical, in the form of a gel, applied at the end of the operation and for home use according to therapeutic scheme prescribed at the time of discharge. Primary objective: To evaluate whether the use of ozone in patients undergoing extraction of impacted third molars reduces post-operative pain 7 days after surgery. Secondary objectives: - Evaluate the functional limitation in opening the mouth (trismus) 7 days after surgery. - Evaluate if there is a reduced intake of analgesic drugs in the 7 days following the operation. - Evaluate the perceived quality of life in the 7 days following the intervention.

NCT ID: NCT05943015 Recruiting - Postoperative Pain Clinical Trials

Analgesic Efficacy of Quadratus Lumborum, Paravertebral Blocks

Start date: September 5, 2022
Phase: N/A
Study type: Interventional

This trial is a prospective, randomized, single-center, single blinded-analysis trial, the objective of which is compare the postoperative analgesia efficacy of Quadratus lumborum II, Quadratus Lumborum III and Paravertebral blocks in elective laparoscopic cholecystectomy.

NCT ID: NCT05941130 Recruiting - Quality of Life Clinical Trials

3D Evaluation of Postoperative Edema After Third Molar Surgery

Start date: July 1, 2022
Phase: Phase 4
Study type: Interventional

Surgical removal of third molars is recognized as one of the most frequent procedures performed in oral surgery. Literature is rich in studies attempting to demonstrate the benefit of corticosteroids in third molar surgery, however the variety of methods, doses, routes and timing of administration has hampered the standardization of their use in light of best evidence. Also the use of 3D facial superimposition methodology to measure and analyze facial swelling after third molar surgery is a relatively new and promising technology.

NCT ID: NCT05936190 Recruiting - Opioid Use Clinical Trials

Comparison of the Effect of Lidocaine Infusion Applied at Different Doses During Lumbar Spinal Surgery on Hemodynamics and Postoperative Pain

Start date: February 10, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effects of intravenous infusion of lidocaine at different doses (1 mg/kg/h vs. 2 mg/kg/h) in the intraoperative period in patients undergoing lumbar stabilization, whether postoperative pain, postoperative opioid use, opioid-related side effects are reduced, and its effects on intraoperative hemodynamics

NCT ID: NCT05934266 Recruiting - Postoperative Pain Clinical Trials

Impact of Mesh Fixation With Tissue Adhesive

Start date: March 29, 2023
Phase: Phase 4
Study type: Interventional

Randomized controlled trial on mesh fixation using cyanoacrylate glue compared to standard suture in open inguinal hernia repair.