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Pain, Postoperative clinical trials

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NCT ID: NCT04244097 Completed - Pain, Postoperative Clinical Trials

The Effect of Intraperitoneal Bupivacaine Versus Bupivacaine With Neostigmine on Pain in Laparoscopic Cholecystectomy

RCTcompstud
Start date: April 10, 2020
Phase: Phase 2
Study type: Interventional

Injection of intraperitoneal bupivacaine revealed an analgesic effect whether injected alone or in combination with other adjuvants, which increase duration of analgesia and decrease the dose of administered bupivacaine thus minimizing its side effects e.g. Opioids, Corticosteroids and Magnesium sulphate. Neostigmine, a cholinesterase inhibitor that produces muscarinic receptor-mediated analgesia, increased postoperative analgesia when combined with local anaesthetics. Peripheral afferent nerve fibres contain muscarinic receptors, these could be a good target for pain suppression.

NCT ID: NCT04243967 Completed - Anxiety Clinical Trials

Music Therapy Pathway in Patients Undergoing Total Laparoscopic Hysterectomy

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

Music therapy is a non-invasive, safe, and inexpensive intervention that can be easily and successfully delivered. it has been shown that music therapy might reduce the postoperative pain in patients undergoing cesarean section and in those with cancer, showing a lower state of anxiety and greater pain reduction in participants who received music interventions. The aim of the present study is to investigate the role of music and music therapy on anxiety and perception of pain in patients undergoing elective hysterectomy for benign disease.

NCT ID: NCT04242407 Recruiting - Pain, Postoperative Clinical Trials

Evaluating Efficacy of the Dexmedetomidine Transdermal System for Postoperative Analgesia Following Abdominoplasty

Start date: July 7, 2020
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the analgesic efficacy of Dexmedetomidine Transdermal System (DMTS), compared with placebo, in participants following abdominoplasty.

NCT ID: NCT04241640 Completed - Pain, Postoperative Clinical Trials

Nefopam for Post Video-Assisted Thoracoscopic Lobectomy

Start date: September 1, 2020
Phase: Phase 4
Study type: Interventional

Video-assisted thoracoscopic (VATs) lobectomy is mild to moderately pain procedure. For conventional thoracotomy, there are many invasive pain control such as epidural analgesia, paravertebral block. However, for VATs, the invasive pain control somehow are too invasive. Nefopam is non-opioid painkilling medication, Serotonin, norepinephrine, dopamine reuptake inhibitor. Many study were demonstrated positive outcome of nefopam usage in many operation such as abdominal surgery, laparocopic surgery, orthopedic surgery. Nevertheless, nefopam for VATs is not well studied yet.

NCT ID: NCT04239794 Active, not recruiting - Anesthesia Clinical Trials

The Influence of Type of Anesthesia on Postoperative Pain

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

The investigators designed a multi-center prospective randomized controlled trial to study the influence of the type of anesthesia on postoperative pain after laparoscopic colorectal cancer surgery. Half of the participants will be anesthetized with propofol and remifentanil, while the other half will be anesthetized with sevoflurane and remifentanil during the surgery. The investigators will measure opioid consumption and pain score in the acute postoperative phase.

NCT ID: NCT04238780 Recruiting - Postoperative Pain Clinical Trials

Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

NCT ID: NCT04236323 Completed - Pain, Postoperative Clinical Trials

The Effect of Remifentanil on Rebound Pain

Start date: February 14, 2020
Phase: N/A
Study type: Interventional

The investigators will evaluate the influence of intraoperative remifentanil infusion on the postoperative hyperalgesia in patients receiving rotator cuff repair after brachial plexus block for postoperative analgesia.

NCT ID: NCT04235530 Completed - Postoperative Pain Clinical Trials

Comparison of Ultrasonography Guided Serratus Anterior Plane Block and Thoracic Paravertebral Block in Thoracic Surgery

Start date: April 15, 2018
Phase:
Study type: Observational [Patient Registry]

The aim of this study is comparison of the effectiveness of ultrasound guided serratus anterior plane block and thoracic paravertebral block as a preventive analgesia method after VATS. Our secondary aim is to investigate patient and surgeon satisfaction, duration of block application, postoperative complications and hospital lenght of stay.

NCT ID: NCT04233736 Recruiting - Clinical trials for Erector Spinae Plane Block

Erector Spinae Plane Blocks (ESP) for Postoperative Pain in Lumbo-sacral Spine Surgery

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

The goal of this study is to evaluate the analgesic efficacy of bilateral erector spinae plane (ESP) blocks after lumbar and lumbo-sacral spine surgery by assessing postoperative pain scores and opiate requirements as the primary outcome measures. We are aiming to investigate how ESP blocks, performed under ultrasound guidance at the T12 vertebral level, contribute to postoperative pain control. This will be determined by measuring numerical rating pain scores repeatedly following surgery and opiate consumption until patient discharge from hospital. These primary outcome measures will be compared between a treatment group of participants, who will receive ESP blocks and a control group who will receive a sham block. Our primary hypothesis is that ESP blocks significantly reduce postoperative pain and opiate requirements

NCT ID: NCT04232306 Withdrawn - Postoperative Pain Clinical Trials

Liposomal Bupivacaine + Bupivacaine vs. Bupivacaine Alone on Opioid Use After Elective c/Section

Start date: March 2024
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effectiveness of local wound infiltration of EXPAREL® (liposomal bupivacaine) with bupivacaine HCl compared to active control with bupivacaine HCl alone following elective primary or repeat cesarean delivery with spinal anesthesia.