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Pain, Postoperative clinical trials

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NCT ID: NCT03673358 Terminated - Pain, Postoperative Clinical Trials

Cognitive Behavioural Therapy to Optimize Post-Operative Recovery Pilot

COPE Pilot
Start date: January 9, 2019
Phase: N/A
Study type: Interventional

Psychological factors such as stress, distress, anxiety, depression, and poor coping strategies may be associated with ongoing pain following injuries such as fractures. To study this relationship, patients will undergo cognitive behavioural therapy (CBT) which is designed to modify such thoughts with the goal of reducing ongoing pain and improving quality of life. The goal of this study is to determine if CBT, versus usual care, reduces the prevalence of moderate to severe persistent post-surgical pain (PPSP) over 12-months post-fracture

NCT ID: NCT03673163 Recruiting - Chronic Pain Clinical Trials

Lidocaine Infusion for Pain After Herniotomy

LIPAH
Start date: November 6, 2018
Phase: N/A
Study type: Interventional

This study seeks to investigate lidocaine infusion to reduce occurrence of chronic postoperative pain at 3-month after inguinal herniotomy

NCT ID: NCT03672669 Completed - Pain, Postoperative Clinical Trials

Comparison of the Effect of A-PRF and L-PRF on Outcomes After Removal of Impacted Mandibular Third Molar

Start date: November 5, 2017
Phase: N/A
Study type: Interventional

In this study, it was aimed to investigating and comparing the postoperative effects of leukocyte- and platelet-rich fibrin (L-PRF) and advanced platelet-rich fibrin (A-PRF) in terms of pain, swelling on the cheek, and trismus after mandibular third molar surgery. The study included a total of 27 patients with bilateral impacted mandibular third molar which surgically operated at different times. Patients were evaluated in two randomly separated groups. For the first group; A-PRF and for the second group; L-PRF was applied into the tooth socket. The outcomes variables were; pain, swelling, the number of analgesics taken, and trismus. These variables were also assessed on the basis of; 1st, 2nd, 3rd and 7th days following the operation.

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: NCT03666299 Recruiting - Chronic Pain Clinical Trials

Lidocaine Infusion for Postthoracotomy Pain Syndrome

LIPPS
Start date: November 6, 2018
Phase: N/A
Study type: Interventional

This study seeks to investigate lidocaine infusion to reduce postthoractomy pain syndrome after thoracic Surgery

NCT ID: NCT03665233 Terminated - Anesthesia Clinical Trials

Virtual Reality for Post Operative Pain Management After Total Knee Arthroplasty

VR4POPKA
Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Virtual reality has been used for acute pain management (burn patients) with positive results. Hypnosis has known beneficial effects on patients in the peri-operative setting. The investigators are combining both by giving a virtual reality hypnosis (VRH) session to the patients during a known painful post-operative moment. (physiotherapy) It is the investigator intention to compare pain after physiotherapy during the first 3 days after a total knee arthroplasty, between 2 groups. One group , the VR group gets standard treatment with VRH and the second, the sham group, gets standard treatment with a sham VR session.

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: NCT03662451 Not yet recruiting - Pain, Postoperative Clinical Trials

Single Site Versus Multi Site Robotic Hysterectomy

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

Robotic single site surgery (R-SSH) is a novel technique, which may be superior to multi site hysterectomy (R-MSH) in select patients regarding cosmesis and postoperative pain. A randomized trial is performed to compare R-SSH with R-MSH with regard to the postoperative rehabilitation, cosmesis, the operational cost, and the perioperative morbidity.

NCT ID: NCT03660020 Recruiting - Postoperative Pain Clinical Trials

Ultrasound Guided Erector Spinae Plane Block in Breast Surgery

Start date: May 19, 2018
Phase: N/A
Study type: Interventional

hyalorounidase will be added to local anaesthetics in patients undergoing mastectomy and effect on local anaesthetic spread will be studied under floroscope