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Pain, Postoperative clinical trials

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NCT ID: NCT04114149 Recruiting - Pain, Postoperative Clinical Trials

Effective Postoperative Pain Relief After Laparoscopic Cholecystectomy With TENS

Start date: March 19, 2019
Phase: N/A
Study type: Interventional

The study evaluates the effect of TENS (transcutaneous electrical nerve stimulation) treatment for first line of treatment compared with conventional treatment with opioids on pain relief and time spent time in the post-anesthesia care unit after laparoscopic cholecystectomy. Half of the patients are randomized to TENS as first line of treatment and the second half is randomized to conventional opioid treatment. Patients who does not report postoperative pain which requires treatment are used as controls.

NCT ID: NCT04111406 Terminated - Postoperative Pain Clinical Trials

Comparison of the Incidence of Inadequate Epidural Analgesia Between Protocol Based and Current Practice

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

Epidural analgesia is the recommended analgesic technique in patients having surgery with severe postoperative pain such as thoracic and upper abdominal surgery. However, from the previous study, the incidence of inadequate pain control in patients receiving epidural analgesia is very high 48.6% in our hospital.

NCT ID: NCT04111302 Not yet recruiting - Clinical trials for Postoperative Pain After Hemorrhoidectomy

Cohort Study of Auricular Acupressure for Postoperative Pain After Hemorrhoidectiomy

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

Auricular pressure is effective for postoperative analgesia after hemorrhoidectomy, but the evidence is not sufficient.

NCT ID: NCT04111081 Enrolling by invitation - Postoperative Pain Clinical Trials

Auricular Pressure for Postoperative Pain After Hemorrhoidectiomy: a Randomized Controlled Trial

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

Auricular pressure is effective for postoperative analgesia after hemorrhoidectomy, but the evidence is not sufficient.

NCT ID: NCT04110886 Completed - Chronic Pain Clinical Trials

Safety, Tolerability, and Pharmacokinetics of HSK21542 in Healthy Volunteers

Start date: July 2, 2020
Phase: Phase 1
Study type: Interventional

This is a A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single-Ascending-Dose Study To Investigate the Safety, Tolerability, and Pharmacokinetics of a kappa receptor agonist HSK21542 in Healthy Volunteers. The study will enroll approximately 50 adults. The anticipated study duration will be up to 6 months.

NCT ID: NCT04110132 Not yet recruiting - Postoperative Pain Clinical Trials

Postoperative Analgesia Using Ganglion Impar Block After Anal Surgery

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the ganglion Impar block in the prevention of postoperative pain after anal surgery.

NCT ID: NCT04110080 Recruiting - Pain, Postoperative Clinical Trials

Enhanced Recovery After Surgery in Kidney Transplant Donors

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

Enhanced recovery after surgery (ERAS) pathways are designed to optimize perioperative management, improving patient outcomes and satisfaction through multimodal techniques. Living kidney transplant donors are typically healthy individuals who undergo laparoscopic nephrectomy. The most significant hindrance to discharge to return to activities of daily living is frequently return of bowel function and postoperative pain. Through a randomized controlled trial design, we will evaluate the effectiveness of implementing an ERAS pathway. We hypothesize that preoperative patient optimization through exercise, carbohydrate loading, and counseling on expectations, in addition to multimodal pain management strategies which limit opioids would allow faster recovery, early bowel function, decreased postoperative pain, increased patient satisfaction and shorter length of stay. The study population will include a total of 42 patients (age 18-80) who are American Society of Anesthesiologists (ASA) Physical Status (PS) 1-3, undergoing living donor nephrectomy. Our primary outcome measures will be postoperative opioid consumption. Secondary outcome measures are: postoperative pain score, time to return of bowel function, ambulation, first oral intake postoperatively, and patient satisfaction scores. Other objectives include reducing readmissions, shorter hospital length of stay and decreased operative complications, including nausea, vomiting and wound infection.

NCT ID: NCT04109638 Recruiting - Pain, Postoperative Clinical Trials

Pulsed Electromagnetic Field (PEMF) Therapy for Post-operative Pain Following Orthopedic Surgery

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

The primary objective of this study is to prospectively determine, at 10 days after orthopedic shoulder or knee surgery, if pulsed electromagnetic field (PEMF) therapy is beneficial in reducing patient-reported post-operative pain, as measured by visual analog scale (VAS). The amount of pain medication taken daily and the physical function outcome scores after surgery and PEMF treatment will also be measured.

NCT ID: NCT04109573 Recruiting - Post Operative Pain Clinical Trials

Function Following Laser for Anal Intraepithelial Neoplasia (FLAN)

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

High-grade squamous intraepithelial lesions (HSIL) and anal cancer are rising in incidence and at highest risk are HIV positive men who have sex with men (MSM). This pilot study assessing anal function and patient-reported outcomes before and after laser ablation of HSIL will add to the evidence that such a therapy is an acceptable and safe treatment to offer in a preventative setting.We will be recruting HIV positive and negative MSM.

NCT ID: NCT04108975 Not yet recruiting - Postoperative Pain Clinical Trials

Assessment of the Effect of Rectus Muscle Reapproximation Versus Non Reapproximation During CS on Postoperative Pain

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to assess the effect of rectus muscle re-approximation by 3 interrupted simple sutures versus tighting it by 3 vertical mattress sutures during cesarean delivery on postoperative pain.