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Pain, Postoperative clinical trials

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NCT ID: NCT00508495 Completed - Pain, Postoperative Clinical Trials

Analgesic Efficacy, Safety and Tolerability of Two Paracetamol-Containing Solutions in Post-Surgical Hip Replacement Pain

Start date: August 2007
Phase: Phase 3
Study type: Interventional

The aim of the study is to evaluate the therapeutic efficacy, safety and local tolerability of two different paracetamol-containing solutions in postoperative total hip replacement. They will be compared to placebo (a dummy treatment which contains no active ingredient).

NCT ID: NCT00508092 Completed - Pain, Postoperative Clinical Trials

Combined Nerve Blockade and Local Infiltration Anesthesia in Appendectomy - A Blinded Randomized Study

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the use of local anesthetic to numb the nerves that run deeper in the abdominal wall gives better post operative pain control than just infiltrating local anesthetic to the wound edges.

NCT ID: NCT00507026 Completed - Postoperative Pain Clinical Trials

Efficacy and Safety of IV Diclofenac (DIV075V)for Pain After Elective Orthopedic Surgery

Start date: July 25, 2007
Phase: Phase 3
Study type: Interventional

This study will compare repeated intermittent IV dosing of diclofenac in patient with moderate to severe post-surgical pain from elective orthopedic surgery.

NCT ID: NCT00500214 Completed - Postoperative Pain Clinical Trials

Ilioinguinal Nerve Excision in Open Mesh Repair of Inguinal Hernia,a Randomized Clinical Trial

Start date: April 2005
Phase: Phase 2
Study type: Interventional

this study was designed to evaluate the effect of routine excision of the ilioinguinal nerve in an attempt to decrease the incidence of chronic inguinodynia in patients who undergo open anterior hernia mesh repair.

NCT ID: NCT00495807 Completed - Postoperative Pain Clinical Trials

Nurses' Negative Words and Postoperative Pain Management

NWPOP
Start date: June 2006
Phase: N/A
Study type: Interventional

Psychological implications expressed pivotal effects on daily activities. Postoperative pain management is always encountered varying influence from the ambience of surgical wards, especially the nurses. We hypothesized that nurses' negative or positive words would produce unexpected role in pain management, which might be a strong factor resulting in the failure of postoperative analgesia.

NCT ID: NCT00493909 Completed - Pain, Postoperative Clinical Trials

Prospective, Randomised, Single-Blinded, Monocentric Clinical Study to Compare Postoperative Analgesia and Outcome After Combined Paravertebral and Intrathecal Versus Thoracic Epidural Analgesia for Thoracotomy

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare whether epidural analgesia would provide equal analgesia than combining intrathecal opioids with thoracic paravertebral local anesthetics.

NCT ID: NCT00492453 Recruiting - Postoperative Pain Clinical Trials

Spinal Versus General Anesthesia for Laparoscopic Cholecystectomy

SALC
Start date: September 2004
Phase: N/A
Study type: Interventional

The purpose of the study is to assess whether spinal anesthesia is or not superior to the standard general anesthesia for fit patients undergoing laparoscopic cholecystectomy.

NCT ID: NCT00488787 Completed - Pain, Postoperative Clinical Trials

Safety and Efficacy of Intranasal Ketamine for the Treatment of Postoperative Dental Pain

Start date: March 2001
Phase: Phase 2
Study type: Interventional

Once patients' postoperative pain intensity reaches a moderate-to-severe level, they are randomized to receive intranasal ketamine or placebo. Patients remain in the study unit for 3 hours post administration and assess pain intensity and pain relief throughout the 3 hour postoperative period.

NCT ID: NCT00485693 Completed - Postoperative Pain Clinical Trials

Dose-Ranging Study for Prolonged Postoperative Analgesia in Subject Undergoing Total Knee Arthroplasty

TKA
Start date: June 2007
Phase: Phase 2
Study type: Interventional

Dose-ranging study for prolonged postoperative analgesia in subjects undergoing total knee arthroplasty

NCT ID: NCT00485667 Completed - Postoperative Pain Clinical Trials

Phase 1 Thorough QT Study in Young Healthy Volunteers

TQT
Start date: June 2007
Phase: Phase 1
Study type: Interventional

A reduction in the postoperative need for opioids to enhance the recovery process and increase patient postoperative satisfaction.