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Pain, Postoperative clinical trials

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NCT ID: NCT02216305 Completed - Pain, Postoperative Clinical Trials

HAL-RAR Versus Hemorrhoidectomy in the Treatment of Grade III-IV Hemorrhoids. Prospective, Randomized Trial

Start date: September 2014
Phase: N/A
Study type: Interventional

HYPOTHESIS 1. HAL- RAR causes a lower immediate postoperative pain compared with excision hemorrhoidectomy. 2. HAL - RAR achieves similar immediate and long term results compared to the excision hemorrhoidectomy in the control of hemorrhoidal symptoms. 3. The complication rate of HAL- RAR is low and similar to excision hemorrhoidectomy. OBJECTIVES 1. Compare postoperative pain of both techniques. 2. Assess the short and long-term control of hemorrhoidal symptoms by HAL- RAR technique, and compare the results with those of the excision hemorrhoidectomy. 3. Evaluate and compare the rate of complications of both techniques. 4. Assess the quality of life of patients before and after treatment.

NCT ID: NCT02211534 Completed - Clinical trials for Post-Operative Pain Following Total Knee Arthroplasty

Pilot Study of PEMF Therapy in Treatment of Post-operative Pain Following Total Knee Arthroplasty

Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether pulsed electromagnetic energy field (PEMF) therapy is effective in the treatment of persistent pain following total knee arthroplasty (TKA)

NCT ID: NCT02210429 Active, not recruiting - Pain, Postoperative Clinical Trials

Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of Single Shot Catheter Techniques

Start date: January 2009
Phase: N/A
Study type: Interventional

We hypothesize that patients who receive a supraclavicular block via Angiocath, placed intra-operatively and dosed post-operatively following neurologic examination, will have lower pain scores, lower use of intravenous morphine equivalents in the post-anesthesia care unit, and lower rates of intervention for post-operative nausea and vomiting. We also hypothesize that patients receiving this nerve block had the same rates of nerve damage as the patients who did not receive a block and that there will be no demonstrable safety concerns with this block.

NCT ID: NCT02209233 Withdrawn - Anxiety Clinical Trials

Effects of Massage on Post-operative Pain in Urologic Patients

Start date: February 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect that receiving massage therapy post-operatively has on reducing perceived anxiety and pain in urology patients. Secondarily, the result of massage on patient satisfaction, length of hospital stay, and narcotic use will also be studied.

NCT ID: NCT02205580 Enrolling by invitation - Tonsillitis Clinical Trials

Continuous Intravenous Sufentanil Infusion for Postoperative Pain Management Following Tonsillectomy or Adeno-tonsillectomy in Children

Start date: September 2014
Phase: Phase 4
Study type: Interventional

Postoperative pain following tonsillectomy or adeno-tonsillectomy in children is severe and sometimes last for days. Sufentanil is used by epidural route for postoperative analgesia in children. There are few reports about its use for postoperative analgesia by continuous intravenous infusion. Its complications include , hypoxia, sedation, pruritus ,nausea and/or vomiting. The investigators design this protocol to test efficacy of analgesia of three different rates of continuous intravenous sufentanil infusion for postoperative pain management following coblation tonsillectomy or adeno-tonsillectomy in children. The investigators also compare incidence rate of complications for three groups.

NCT ID: NCT02204878 Recruiting - Laparotomy Surgery Clinical Trials

Role of Parecoxib Sodium for Postoperative Pain Management in Open Hepatectomy

Start date: July 2014
Phase: Phase 4
Study type: Interventional

To searching the role of parecoxib sodium for postoperative pain management in open hepatectomy

NCT ID: NCT02200016 Completed - Postoperative Pain Clinical Trials

Displacement of Popliteal Sciatic Nerve Catheters After Major Foot and Ankle Surgery

Start date: November 2014
Phase: Phase 4
Study type: Interventional

Displacement of popliteal sciatic nerve catheters after major foot and ankle surgery. A randomized controlled double blinded MRI study comparing long versus short axis catheter placement. Which procedure for insertion of nerve catheters for postoperative pain after major foot and ankle surgery is the best

NCT ID: NCT02198235 Completed - Postoperative Pain Clinical Trials

Prolonged Popliteal Fossa Nerve Blockade (Prolonged Pop)

Start date: October 2012
Phase: Phase 1
Study type: Interventional

This study looks at addition of medications to the local anesthetic for the nerve blockade.

NCT ID: NCT02197156 Completed - Postoperative Pain Clinical Trials

A Multicenter Active Comparator Study of HC-ER in Adults Following Bunionectomy Surgery

Start date: August 2002
Phase: Phase 2
Study type: Interventional

The purpose of the study is to establish a dose-response relationship among several capsule strengths of Hydrocodone Bitartrate Extended Release (HC-ER) and to compare the efficacy to placebo following bunionectomy surgery

NCT ID: NCT02196727 Completed - Postoperative Pain Clinical Trials

Evaluation of Postoperative Pain Following Bascom Cleft Lift Operation

Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to evaluate postoperative pain in Bascom Cleft Lift operation receiving multimodal analgesia in day-case surgery setting. Hypothesis: Multimodal analgesia provides adequate pain relief in patients undergoing Bascom Cleft Lift operation.