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Pain, Postoperative clinical trials

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NCT ID: NCT04362566 Completed - Pain, Postoperative Clinical Trials

Bupivacaine for Post-operative Pain in Mohs

Start date: July 30, 2020
Phase: Phase 4
Study type: Interventional

Mohs micrographic surgery (MMS) is regarded as the gold standard for the treatment of high-risk nonmelanoma skin cancer (NMSC). Pain after MMS peaks on the day of surgery and slowly decreases thereafter. The most common post-operative analgesics include acetaminophen, ibuprofen and narcotics. Lidocaine is the most commonly used anesthetic in MMS, but bupivacaine has been shown in other surgical specialties to be an effective adjuvant to reduce post-operative pain and opioid use when injected locally in the immediate postoperative period. Bupivacaine has also been shown to reduce intra-operative pain during MMS. The investigators plan a single-blinded prospective, randomized, controlled trial to determine if post-operative wound infiltration of bupivacaine versus normal saline improves post-operative pain and decreases need for post-operative pain medications including both narcotic and nonnarcotic analgesics.

NCT ID: NCT04360135 Withdrawn - Post Operative Pain Clinical Trials

Preemptive Acetaminophen for Postoperative Pain Control Following Minimally Invasive Hysterectomy

Start date: May 6, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

This study is investigating whether administration of acetaminophen the day before surgery improves post operative pain following minimally invasive hysterectomy. Patients will receive either acetaminophen or placebo to take twice per day the day prior to their scheduled surgery. The morning of surgery all participants will receive oral acetaminophen at least 30 minutes prior to surgery. The investigators will examine whether there is a difference in post operative pain between the two groups.

NCT ID: NCT04357132 Completed - Pain Clinical Trials

Virtual Reality for Appendectomy Pain

Start date: July 12, 2020
Phase: N/A
Study type: Interventional

To determine the impact of VR-Biofeedback and VR-Distraction on pain and medication utilization in children and adolescents undergoing surgery for ruptured appendix.

NCT ID: NCT04351776 Completed - Pain Clinical Trials

Virtual Reality and Pain

FOREVR Peds
Start date: July 10, 2020
Phase: N/A
Study type: Interventional

Determine the impact of VR-Biofeedback, VR-distraction, and 360 video on pain and medication utilization in patients undergoing surgery; determine the role of anxiety and pain catastrophizing on changes in pain following VR-BF in patients undergoing surgery.

NCT ID: NCT04349774 Withdrawn - Pain, Postoperative Clinical Trials

Erector Spinae Plane Block vs Erector Spinae Plane Block With Serratus Anterior Plane Block in Thoracic Surgery

Start date: October 1, 2022
Phase: Phase 4
Study type: Interventional

This pilot study will prospectively compare continuous Erector Spinae Plane block (ESP) versus combination of continuous Erector Spinae Plane block and single shot Serratus Anterior Plane block for post-operative pain management in subjects undergoing primary thoracic surgery.

NCT ID: NCT04349397 Active, not recruiting - Pain, Postoperative Clinical Trials

Use of Analgesics and Pain Scores After Pediatric Adenotonsillectomy

Start date: August 1, 2019
Phase:
Study type: Observational

The purpose of the study is to quantify the use of pain medications given to children aged 3 - 12 years as well as their pain level through pain scores after they have undergone a tonsillectomy or adenotonsillectomy surgery at Doernbecher Children's Hospital (DCH). We would like to learn more about the pain medications given and the pain scores of children post-surgery for the first 5 days following discharge from the hospital.

NCT ID: NCT04346758 Completed - Postoperative Pain Clinical Trials

Ultrasound-assisted Shamrock Method for Lumbar Plexus Nerve Block in Elderly Trauma Patients, Revisited.

Start date: February 15, 2020
Phase: N/A
Study type: Interventional

A revised ultrasound-guided approach to the lumbar plexus is investigated as for efficacy and safety in elderly trauma patients undergoing operations of the lower extremeties.

NCT ID: NCT04346407 Enrolling by invitation - Post-operative Pain Clinical Trials

Dronabinol for Post-operative Pain After Lumbar Fusion

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

Impact of 2.5mg of oral Dronabinol daily versus placebo on post-operative opioid consumption on patients aged 18 to 65 years old undergoing 1 to 3 level posterolateral fusion

NCT ID: NCT04344990 Completed - Postoperative Pain Clinical Trials

Postoperative Pain Management After Total Knee Arthroplasty

Start date: June 29, 2015
Phase: N/A
Study type: Interventional

The study compares three different analgesic techniques in order to determine which one serves as the optimal method for postoperative pain management after Total Knee Arthroplasty in patients suffering from Osteoarthritis

NCT ID: NCT04343937 Completed - Postoperative Pain Clinical Trials

Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery

Start date: April 15, 2020
Phase:
Study type: Observational

This retrospective study included 30 patients scheduled for lumbar herniectomy under general anesthesia. The patients were randomized to receive either retrolaminar block or intravenous analgesia treatment.Numeric Pain Rating Scale (NPRS) was used to measure the pain intensity of patients in postoperative period. Postoperative analgesic requirements were recorded to asses effectiveness of regional anesthesia.Opiod and NSAİD as rescue medication were recorded postoperatively.