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Pain, Postoperative clinical trials

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NCT ID: NCT05831501 Completed - Post Operative Pain Clinical Trials

Postoperative Analgesic Efficacy of Trans Abdominis Plane Block

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Transverse abdominis plane (TAP) block is an effective method to manage postoperative pain in patients with midline abdominal wall incisions. It is used frequently in many lower abdominal surgeries however its use after caesarean section is still new, and fewer studies are available. We conducted this study to see the analgesic effect of TAP block after caesarean section.

NCT ID: NCT05831449 Recruiting - Bunion Clinical Trials

CPL-01 in the Management of Postoperative Pain After Bunionectomy

Start date: May 22, 2023
Phase: Phase 3
Study type: Interventional

Subjects receive study drug during bunionectomy and are followed for pain and opioid use, with the hypothesis that those who receive CPL-01 will have less pain and less opioid use than either control arm.

NCT ID: NCT05831345 Recruiting - Orthopedic Surgery Clinical Trials

Intraoperative Methadone for the Prevention of Postoperative Pain

Start date: February 28, 2023
Phase: Phase 3
Study type: Interventional

The pain felt after orthopedic surgery in the absence of adequate locoregional anesthesia is often insufficiently controlled, especially during the first 24 hours postoperatively. Methadone, due to its long half-life, may provide better pain control after orthopedic surgery when associated locoregional anesthesia cannot be performed. It may be impossible to perform loco-regional anesthesia in various contexts: patient refusal, pre-existing neurological impairment, infection at the injection site, coagulopathies, inability to cooperate, total language barrier, allergy to anesthetics, unavailability of equipment (ultrasound, etc.) or equipped room, lack of experience of nursing staff in performing the block and in the postoperative management of the patient. Intraoperative administration of methadone in these settings may be superior to sufentanil for pain control during the 24 hours post orthopedic surgery, and the pain control provided by methadone does not appear to imply a higher likelihood of adverse events related to opioids.

NCT ID: NCT05830513 Not yet recruiting - Pain, Postoperative Clinical Trials

OPU-LUX: Virtual Reality for Pain and Anxiety Management During Oocyte Pick-up

OPU-LUX
Start date: May 2023
Phase: N/A
Study type: Interventional

In vitro fertilization (IVF) cycles are increasingly performed worldwide. Transvaginal oocyte pick-up (OPU) is a painful part of IVF. OPU in polyfollicular IVF is usually performed under sedation and pain relief. In natural cycle IVF or IVF with minimal stimulation OPU is possible without anesthesia. Mostly of the women reported experiencing mild to moderate pain when undergoing OPU without anesthesia. Nevertheless, there is a need for alternative pain treatment options during OPU to reduce the burden of IVF for patients. Virtual reality (VR) may have a role in acutely painful procedures as a non-pharmacological alternative. VR refers to the interactions between an individual and a computer-generated environment stimulating multiple sensory modalities. The immersive, entertaining effects of VR could be useful for redirecting the patient's attention away from painful treatment experiences and reducing anxiety, discomfort, or unpleasantness. Use of VR interventions has been studies in a wider range of medical treatment.

NCT ID: NCT05826093 Completed - Postoperative Pain Clinical Trials

Cutaneous Sensory Block Area of the Subcostal Ultrasound-Guided Transversus Abdominis Plane Block

CUSBAT
Start date: February 15, 2022
Phase:
Study type: Observational

Patients planned for elective laparoscopic cholecystectomy received a peroperative ultrasound-guided subcostal transversus abdominis plane block (USTAP) at the beginning of the procedure. At T90 minutes after the end of anaesthesia the cutaneous sensory block area (CSBA) was measured using cold sensation and mapped with a sterile marker. The CSBA was photodocumented and the area calculated.

NCT ID: NCT05825495 Not yet recruiting - Pain, Postoperative Clinical Trials

Postoperative Pain Management on Uvulopalatopharyngoplasty Patients

Start date: May 1, 2023
Phase: Phase 4
Study type: Interventional

This is a randomized controlled study, aimed to investigate the effects of dinalbuphine sebacate (DS) on patients having uvulopalatopharyngoplasty (UPPP). DS is a prodrug of nalbuphine, a mixed agonist-antagonist opioid. The mean absorption time for the complete release of DS into systemic circulation is approximately 145 h, which could theoretically provide extended analgesic effects for up to 6 days. Patients diagnosed with obstructive sleep apnea are generally associated with higher risks towards opioid side effects, especially respiratory depression. Post-UPPP pain managing should be cautiously arranged and executed. We hypothesize that the combination of our routine practice and DS will improve the outcomes after Uppp.

NCT ID: NCT05824832 Recruiting - Pain, Postoperative Clinical Trials

Buprenorphine, Clonidine, and Dexamethasone on Duration of Brachial Plexus Blocks for Upper Extremity Surgery

Start date: February 28, 2023
Phase: Phase 4
Study type: Interventional

The goal of this clinical trial is to learn if there is a difference in morphine requirements in patients after upper extremity surgeries including shoulder arthroscopy. The main question it aims to answer is whether there is a difference between Interscalene brachial plexus blocks with the addition of buprenorphine, dexamethasone, and clonidine and the same block without the adjuvant.

NCT ID: NCT05823363 Recruiting - Postoperative Pain Clinical Trials

Vaginal Cuff Infiltration With Liposomal Bupivacaine for Pain Relief: A Double Blind, Randomized Controlled Trial

Start date: April 10, 2023
Phase: Phase 4
Study type: Interventional

The goal is to find out if Exparel (liposomal bupivacaine) given as an injection decreases pain score if given into the vaginal cuff right before starting the minimally invasive (robotic-assisted or laparoscopic) total hysterectomy in patients scheduled for benign indication? Participants will write down 1. pain score at various intervals 2. pain medication used Treatment patients will receive 1)intervention arm will receive Exparel mixed with bupivicaine 2)control arm will receive bupivicaine only

NCT ID: NCT05822011 Recruiting - Post Operative Pain Clinical Trials

Ultrasound Guided Rhomboid Intercostal Subserratus Plane Block vs Erector Spinae Plane Block in Open Nephrectomy

Start date: April 20, 2023
Phase: N/A
Study type: Interventional

Our aim is to measure the efficacy of rhomboid intercostal subserratus plane block and erector spinae plane block in comparison to thoracic epidural block in patients undergoing open nephrectomy

NCT ID: NCT05821725 Recruiting - Palatal Wound Clinical Trials

Effects of Topical Hyaluronic Acid Gel on Postoperative Pain and Wound Healing

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

This clinical study aims to investigate the impact of a topical hyaluronic acid (HA) gel on postoperative pain and wound healing at palatal donor sites in patients undergoing mucogingival procedures involving a de-epithelialized gingival graft (DGG) from the palate. The study design is a Phase III, randomized, double-blind, parallel-group, clinical trial, conducted in a single center, with 30 subjects aged 18-70 years.