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Pain, Postoperative clinical trials

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NCT ID: NCT03669081 Completed - Pain, Postoperative Clinical Trials

Study Evaluating the Effects of Toradol and Lyrica for Pain Control After Donor Nephrectomy

Start date: September 20, 2016
Phase: Phase 2
Study type: Interventional

The investigators will assess how the use of toradol and pregabalin affects return to bowel function and see if there is a difference in length of hospital stay. Narcotic use can affect bowel function so the investigators hypothesize that use of Toradol will decrease delayed bowel function and aid in a patients discharge and reduction of hospital stay.

NCT ID: NCT03667001 Completed - Pain, Postoperative Clinical Trials

Comparing Analgesic Efficacy of Systemic Lidocaine Against Placebo in General Anesthesia in Bariatric Surgery

COALAS
Start date: November 16, 2018
Phase: Phase 3
Study type: Interventional

The investigators plan to evaluate the analgesic effect of systemic Lidocaine in addition to general anesthesia during bariatric surgery. Patients will be subdivided into a "Lidocaine group" and a "Control group". The primary outcome will be the proportion of patients suffering from higher pain intensity within the first four hours after bariatric surgery. Secondary outcomes include the average maximal pain intensity during first four hours and during 48 hours, total opiate consumption, occurence of postoperative nausea and vomiting, time to first defecation and total time spent in hospital.

NCT ID: NCT03663478 Completed - Postoperative Pain Clinical Trials

Continuous TQL Block for Elective Cesarean Section

Start date: September 4, 2018
Phase: Phase 4
Study type: Interventional

The aim of this study is to investigate whether it is possible to prolong time to first opioid with the TQL block by inserting catheters bilaterally, providing continuous analgesia, in patients undergoing elective CS. Our hypothesis is that it will be possible to significantly extend time to first opioid with the blockade by 66.6%, increasing it from a mean of 5.6 hours to a mean of 10 hours.

NCT ID: NCT03657407 Completed - Pain, Postoperative Clinical Trials

B&O for TLH Post-operative Pain and Nausea

Start date: June 1, 2016
Phase: Phase 4
Study type: Interventional

A prospective, single-center, double-blind, randomized, placebo-controlled trial to assess the impact of immediate post-operative placement of a Belladonna and Opium (B&O) rectal suppository on postoperative pain and nausea following laparoscopic and robot-assisted hysterectomy.

NCT ID: NCT03657173 Completed - Pain, Postoperative Clinical Trials

Ultrasound Image Quality of the Brachial Plexus at the Interscalene Space Before and After Shoulder Arthroscopy

Start date: June 18, 2018
Phase:
Study type: Observational

Ultrasound guided interscalene nerve blockade with local anesthesia is a standard regional anesthetic technique for providing postoperative analgesia during shoulder arthroscopy and wide variety of shoulder procedures. There is a paucity of data regarding the effects of shoulder arthroscopy on ultrasound image quality, including the effects of muscle mobilization and the use of large volume irrigation and subsequent tissue absorption, though increased neck circumference and airway edema are known complications of arthroscopic shoulder procedures. The objective of the study is to determine if there is a difference in ultrasound image quality of the interscalene block anatomy, by Likert scale, pre- versus post-operatively in a cohort of patients undergoing shoulder arthroscopy who routinely receive blockade of the brachial plexus for postoperative analgesia. Further, if there are differences in imaging quality, correlations with surgical and patient factors will be studied.

NCT ID: NCT03653988 Completed - Breast Cancer Clinical Trials

Comparison of Pre-op and Post-op Pectoralis Nerve Block

Start date: March 12, 2019
Phase: N/A
Study type: Interventional

The investigators will compare whether patients will have better pain control if they were to receive (PEC I/II block) before surgery or after mastectomy.

NCT ID: NCT03652103 Completed - Pain, Postoperative Clinical Trials

Efficiency of Erector Spinae Plane Block For Patients Undergoing Percutaneous Nephrolithotomy

Start date: September 5, 2018
Phase: Phase 4
Study type: Interventional

Investigators' goal is to determine whether Erector Spinae Plane Block would provide a better analgesia, help mobilization and early discharge or increase satisfaction for patients undergoing Percutaneous Nephrolithotomy(PNL). One of the two groups will receive ESP catheterization after general anesthesia conducted. The other group will receive routine analgesia protocol used for PNL. The total amount of drugs administered, pain scores(NRS) at certain time intervals and at certain events(removal of nephrostomy and pain at mobilization) will be recorded and compared.

NCT ID: NCT03650998 Completed - Postoperative Pain Clinical Trials

Transmuscular Quadratus Lumborum Block for Total Laparoscopic Hysterectomy.

Start date: September 28, 2018
Phase: Phase 4
Study type: Interventional

Study is designed to assess the effect of the transmuscular quadratus lumborum block on postoperative opioid consumption and pain for patients undergoing laparoscopic hysterectomy. Study is randomized, placebo-controlled and blinded. Seventy patients will be included.

NCT ID: NCT03648008 Completed - Pain, Postoperative Clinical Trials

Postoperative Analgesic Effect of Hydromorphone on Partial Pulmonary Resection Under Video-assisted Thoracoscopy

Start date: May 5, 2018
Phase: Phase 4
Study type: Interventional

Postoperative pain remains relatively high within 48h for Chinese patients who receive video-assisted thoracoscopic surgery. Multimodal analgesia combines several agents and/or techniques to function on diverse nociceptive mechanisms to enhance pain relief and lessen side effect. Hydromorphone is a hydrogenated ketone of morphine and approximately 5-10 times more potent. There lacks about efficacy and efficiency of hydromorphone in electrical pump for patient controlled intravenous analgesic (PCIA).

NCT ID: NCT03646630 Completed - Pain, Postoperative Clinical Trials

Quadratus Lumborum Block Versus Caudal Block for Pediatric Postoperative Analgesia

Start date: May 2, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to compare between two regional analgesic techniques; caudal block and ultrasound guided quadratus lumborum block as regard degree of pain relief, accuracy of block, effect on hemodynamic stability and incidence of complications.