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Postoperative Pain clinical trials

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NCT ID: NCT02390804 Completed - Postoperative Pain Clinical Trials

Postoperative Pain After Total Laparoscopic Hysterectomy: a Comparison of Single-port and Three-port Laparoscopy

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

The objective of this study is to compare postoperative pain between single-port access total laparoscopic hysterectomy (SPA-TLH) using a transumbilical single-port system and conventional multi (three)-port access total laparoscopic hysterectomy (MPA-TLH). A prospective study was conducted on women who underwent SPA-TLH and MPA-TLH for benign gynecologic diseases from March 2014 through January 2015. The study enrolled 60 patients and postoperative pain and operative outcomes were examined.

NCT ID: NCT02389907 Withdrawn - Postoperative Pain Clinical Trials

Association Between Patients' Perceptions of Success in Post-op Pain Management and Overall Experience With Care

Start date: June 2015
Phase:
Study type: Observational [Patient Registry]

Assessing the association between patients' perceptions of success with post-operative pain management and overall experience with care.

NCT ID: NCT02380001 Completed - Postoperative Pain Clinical Trials

Analgesic Preoperative/Postoperative Dexketoprofen Trometamol in Third Molar Surgery

Start date: January 2015
Phase: Phase 4
Study type: Interventional

The purpose of the present investigation is to evaluate the effectiveness of the preoperative administration of Dexketoprofen Trometamol, employing the third molar surgery model, when compared to postoperative administration of the same drug. It was hypothesized that preoperative oral Dexketoprofen trometamol will reduce the intensity of pain by 30% after 8 hours of the surgery, when compared with post-operative administration.

NCT ID: NCT02365753 Completed - Postoperative Pain Clinical Trials

Effect of Pulsed Electromagnetic Field Therapy on Pain After Cesarean Delivery

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

A double-blinded randomized control study using a pulsed electromagnetic field therapy to establish whether this device decreases patient pain and decreases narcotic use in women who have undergone cesarean delivery.

NCT ID: NCT02364167 Completed - Postoperative Pain Clinical Trials

Acupuncture for Pain Control After Elective Caesarean Section

ACUSEC
Start date: January 13, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The study entitled "Acupuncture vs. placebo acupuncture and vs. standard therapy for pain control after elective caesarian section - a randomized controlled trial" aims to investigate whether acupuncture with indwelling fixed needles reduces pain and analgesic requirement as compared to placebo and standard therapy in patients after after elective caesarian section (CS) in the period from January 2015 to May 2016. For that purpose 180 adult patients scheduled to elective elective CS in spinal anesthesia will be recruited according to eligibility criteria. 120 patients will be randomized either to verum or placebo acupuncture, 60 patients will be included in non-randomized "standard therapy" arm. The outcome measures are: postoperative analgesic requirement, pain intensity, incidence of side effects and physiological parameters.

NCT ID: NCT02359110 Completed - Postoperative Pain Clinical Trials

Administration of Pre-Operative Gabapentin to Patients Undergoing Laparoscopy

Gabapentin
Start date: June 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to prospectively determine the influence of immediate pre-operative gabapentin administration on acute postoperative pain. The investigators hypothesize that immediate post-operative pain will be improved with pre-operative administration of gabapentin.

NCT ID: NCT02340052 Completed - Postoperative Pain Clinical Trials

Pain Map DK: a Prospective Cohort Study of Pain Treatment in 500 Hip Arthroplasty Patients at Different Danish Hospitals

Start date: April 2014
Phase: N/A
Study type: Observational

This is a prospective observational cohorte study. The aim is to investigate actual pain treatment and outcomes in a large population of total hip arthroplasty patients at 5 different hospitals in Denmark.

NCT ID: NCT02339766 Terminated - Postoperative Pain Clinical Trials

Quadratus Lumborum Block for Post-Cesarean Analgesia

Start date: October 1, 2015
Phase: N/A
Study type: Interventional

Most women having planned cesarean section receive spinal anesthetic for the procedure. Typically, spinal opioids are administered during the same time as a component of multimodal analgesia to provide pain relief in the 16-24 hr period postoperatively. However, spinal opioids are frequently associated with adverse effects such as nausea, pruritus, sedation and occasionally respiratory depression. The quadratus lumborum (QL) block is a regional analgesic technique which blocks T5-L1 nerve branches and has an evolving role in postoperative analgesia for lower abdominal surgeries and is a potential alternative to spinal opioids. There is some evidence that it may provide visceral along with somatic pain relief. It is a simple and safe technique that has been studied in lower abdominal surgeries, but has not been studied for pain relief after cesarean section. If found effective, it will have the advantage of a reduction in opioid associated adverse effects while providing similar quality of analgesia. This block has evolved from the previously known transversus abdominis plane block. We propose to undertake a study that will compare the relative efficacy of QL block with local anesthetic to spinal morphine. We will also study if it provides any incremental benefit when administered in addition to spinal morphine.

NCT ID: NCT02331576 Recruiting - Postoperative Pain Clinical Trials

Analgesic Effect of Perineural Fentanyl Additive to Local Anesthetics in Femoral Nerve Block

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

The purpose of this study is to evaluate the analgesic efficacy of perineural fentanyl combined with local anesthetics in the post operative pain control with continuous femoral nerve block after total knee arthroplasty.

NCT ID: NCT02328378 Completed - Postoperative Pain Clinical Trials

Postoperative Pain Relief After Cesarean Section: Is There a Role for the Quadratus Lumborum Block?

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

The Quadratus Lumborum block (QLB) was first described by Blanco in 2007. The main advantage of QLB compared to the Transversus Abdominis Plane block (TAP) is the extension of local anesthetic agent beyond the TAP plane to the thoracic paravertebral space. The wider spread of the local anesthetic agents produces extensive analgesia and prolonged action of the injected local anesthetic solution. Previous studies showed that TAP block may not be effective in improving postoperative analgesia in patients who had cesarean section under spinal anaesthesia. The aim of this randomised controlled, double blinded study is to examine the effect of QLB on the postoperative pain management in patients who had cesarean section under spinal anesthesia.