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Post-operative Pain clinical trials

View clinical trials related to Post-operative Pain.

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NCT ID: NCT05094323 Recruiting - Post Operative Pain Clinical Trials

Analgesia After Video-Assisted Thoracic Surgery

Start date: February 18, 2022
Phase: Phase 2
Study type: Interventional

Although less invasive, postoperative analgesia remains challenging in patients undergoing uniportal video-assisted thoracic surgery (VATS).

NCT ID: NCT05072184 Completed - Post Operative Pain Clinical Trials

the Effect of Erector Spinae Plane Block on Fentanyl Consumption During Abdominal Hysterectomy

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

This study aims to evaluate the effects of erector spinae plane block on intraoperative fentanyl consumption in patients undergoing abdominal hysterectomy under general anesthesia. To our knowledge, no study in the literature demonstrates this effect.

NCT ID: NCT04999670 Not yet recruiting - Pregnancy Related Clinical Trials

Fascial Closure and Post-caesarean Pain

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

This study will evaluate post-operative pain in patients undergoing elective caesarean sections based on the method of fascial closure. Patients will be randomised into one of three groups based upon the method of fascial closure and will be followed up over a 10 week period evaluating analgesia use in the acute setting, and also following up with pain scores using a visual analogue score throughout the follow-up period.

NCT ID: NCT04988893 Completed - Post Operative Pain Clinical Trials

Quality of Recovery Scores in Parturients With Obesity

Start date: August 9, 2021
Phase:
Study type: Observational

The prevalence of obesity has increased dramatically recently. Obesity is a pro-inflammatory state which leads to chronic low grade inflammation having different systemic effects. This may make obesity an independent risk factor for severe acute postoperative pain. No prospective studies have been conducted to specifically evaluate the quality of recovery after caesarean delivery for women with morbid obesity when compared to non-obese parturients. In addition, while there is biological plausibility to infer worse pain scores in parturients with obesity, the magnitude of this difference is unknown and information guiding adjustments in pain management are lacking.

NCT ID: NCT04964180 Completed - Post-Operative Pain Clinical Trials

Rectal Indomethacin Versus Intraperitoneal Lidocaine for Analgesia After Laparoscopic Cholecystectomy

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

Hospitals, Qena, Egypt in period between May 2020 to May 2021.eighty patients was scheduled to elective laparoscopic cholecystectomy , divided Into two groups randomly using closed envelop method. Group IP lidocaine(40 patients ) received 200 ml saline containing 200 mg 2%lidocaine immediately after abdominal cO2 insufflation( pneumoperitoneum) the surgeon sprayed the total solution on the upper surface of the liver under the right subdiaphragmatic space, left subdiaphragmatic space and around the cholecystectomy site , all patients were maintained in trendelenberg position. At the end of the laparoscopic procedure, group indomethacin (40 patients) recived two 100 mg indomethacin rectal suppositories 2 hours prior to surgery

NCT ID: NCT04963816 Completed - Post Operative Pain Clinical Trials

Pediatric Postoperative Analgesia With Quadratus Lumborum Block(QLB) And Dexamethasone As An Adjuvant To Bupivacaine.

QLB
Start date: June 16, 2021
Phase: N/A
Study type: Interventional

Studying the post-operative analgesic effect of dexamethasone as an adjuvant to bupivacaine giving intravenously and locally with ultrasound guided quadratus lumborum block(QLB) in pediatrics undergoing abdominal surgeries

NCT ID: NCT04911062 Completed - Post-Operative Pain Clinical Trials

HTX-011 in Spinal Surgery

Start date: April 7, 2022
Phase: Phase 2
Study type: Interventional

This is a Phase 2, multicenter study in subjects undergoing an open lumbar decompression surgery.

NCT ID: NCT04909060 Recruiting - Post Operative Pain Clinical Trials

Does the Newborn Infant Parasympathetic Evaluation (NIPE) Index Predict Postsurgical Pain in Children

NIPE
Start date: September 1, 2021
Phase:
Study type: Observational

An investigation to find out if Newborn Infant Parasympathetic Evaluation (NIPE) index predicts postsurgical pain in children, since NIPE is thought to may be of guide to the appropriate therapy in a timely and objective manner, thereby improving patient safety, parental satisfaction, and reducing healthcare costs. We think that, validating the utility of NIPE in children under 3 years of age will allow the implementation of a novel pain assessment tool to our current practice of anesthetic care. This will improve the perioperative pain management, in particular for patients who are unable to communicate pain, with the potential to reduce detrimental consequences of postoperative pain. And also determining the relationship between the NIPE scores and validated FLACC scale for post-operative pain and PAED scale during the recovery from anesthesia and also to determine whether NIPE values at extubation correlates with the incidence of moderate and/or severe pain in PACU.

NCT ID: NCT04848363 Recruiting - Post Operative Pain Clinical Trials

Analgesic Effect of Quadratus Lumborum Block in Laparoscopic Hemicolectomy

Start date: June 16, 2021
Phase: N/A
Study type: Interventional

Comparison of the effectiveness: Quadratus lumborum (QL) block by levobupivacaine with placebo.

NCT ID: NCT04789343 Completed - Post Operative Pain Clinical Trials

The Effect of Instrumentation and Obturation on Postoperative Pain in Retreatment

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

Objectives: The aim of this study was to assess postoperative pain in prospective randomized clinical trial comparing Reciproc or hand instrument and also different obturation techniques in one visit of endodontic retreatment. Conventional root canal treatment was done to 45 patients who needed retreatment. All instruments used in this study are routinely used instrument in endodontic therapy. After completed root canal treatment, the patients asked the intense of post operative pain.