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Pain clinical trials

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NCT ID: NCT01535326 Completed - Pain Clinical Trials

Comparing Water Immersion and Water Exchange Methods During Minimally Sedated Colonoscopy

Start date: February 2012
Phase: N/A
Study type: Interventional

In minimally sedated Asian patients in a community setting the investigators showed that a limited volume of water infusion instead of air insufflation in either the rectal sigmoid colon or the whole colon significantly reduced pain score during colonoscopy. Cecal intubation rate was not compromised. The reduction of pain score ranges from 25% to 32 % in our previous studies.1, 2 In contrast, several US reports described the successful use larger volumes of water infused throughout the entire colon in patients undergoing colonoscopy which result in a greater reduction of the pain score, averaging about 56%.3-5 A recent review suggested that the cause of the difference might lies in the timing of water removal.6 Specifically, the investigators group removed the infused water predominantly during withdrawal phase (water immersion) and the U.S. group removed water during insertion phase (water exchange). This prospective, randomized controlled trial compared water exchange or water immersion with traditional air insufflation in patients undergoing minimally sedated colonoscopy. The investigators test the hypothesis that water exchange can reduce more pain than water immersion in the investigators clinical setting.

NCT ID: NCT01535066 Completed - Breast Cancer Clinical Trials

S1200: Acupuncture, Sham Acupuncture, or Wait List for Joint Symptoms Related to Aromatase Inhibitors in Pts W/Early-Stage Breast Cancer

Start date: May 16, 2012
Phase: N/A
Study type: Interventional

RATIONALE: Acupuncture may help relieve joint pain. PURPOSE: This randomized phase III trial studies acupuncture to see how well it works compared to sham acupuncture or waitlist in treating patients with joint pain related to aromatase inhibitors in patients with early-stage breast cancer.

NCT ID: NCT01533428 Completed - Pain Clinical Trials

A Study to Evaluate Efficacy and Safety of a Single Application of Capsaicin 8%Transdermal Delivery System Compared to Placebo in Reducing Pain Intensity in Subjects With Painful Diabetic Peripheral Neuropathy (PDPN)

STEP
Start date: February 2012
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess efficacy and safety of a single treatment of Capsaicin 8% transdermal delivery system in reducing pain from damaged nerves (neuropathic pain) caused by diabetes.

NCT ID: NCT01532895 Completed - Pain Clinical Trials

Clinical Usefulness and Quality of Life of OROS Hydromorphone in Patients Who Have Not Been Treated With a Strong Opioid

Start date: September 2011
Phase: Phase 4
Study type: Observational

The primary purpose of this study is to evaluate the usefulness of hydromorphone to treat cancer pain in patients who have not been treated with a strong opioid.

NCT ID: NCT01532531 Completed - Pain Clinical Trials

The Effects of Collateral Meridian Therapy for Knee Osteoarthritis Pain Management

Start date: March 2011
Phase: N/A
Study type: Interventional

Collateral meridian therapy (CMT) is a recently developed technique according to traditional Chinese medicine (TCM) experiences, differing from traditional Chinese acupuncture in numerous manners. CMT involves the manipulation of a distant non-painful collateral meridian, thereby facilitating the dissipation of pain. The technique avoids direct stimulation of the involved meridian, which enhances patient tolerability and prevents further injury to the disease and painful areas. Numerous clinical cases have reported the effectiveness of CMT in pain management. This study tests whether CMT is effective for treating knee OA pain and functional recovery.

NCT ID: NCT01531400 Completed - Pain Clinical Trials

Investigation of Pain and Anxiety During Electrodiagnostic Examination Using Self-selected Music

Start date: December 2002
Phase: N/A
Study type: Interventional

The investigators hypothesized that self-selected music played during electrodiagnosis is effective in relieving the discomfort caused by the procedures.

NCT ID: NCT01529671 Completed - Pain Clinical Trials

A Safety And Tolerability Study Of PF-05089771 In Healthy Subjects And In Subjects With Otseoarthritis Of The Knee

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

The purpose of the study is primarily to determine the safety and toleration and pharmacokinetics of PF-05089771 following escalating multiple doses lasting for 14 days.

NCT ID: NCT01529190 Completed - Pain Clinical Trials

Pregabalin on Interleukin-6 Levels in Living Donor Kidney

Start date: March 2011
Phase: Phase 2
Study type: Interventional

Pregabalin, a ligand for alfa2delta subunits of voltage-gated calcium channels, has been shown to be an effective adjuvant therapy for acute postoperative pain, by inhibiting central sensitization. The IL-6, is detectable 60 minutes after surgical incision, persisting for until 10 days, with maximal plasmatic level in 4 and 6 hours. The objective of this study is evaluating the analgesic effect of pregabalin and its repercussion on serum levels of IL6.

NCT ID: NCT01526668 Completed - Pain Clinical Trials

Follow-up Strategies for Improved Postoperative Recovery After Benign Hysterectomy

POSTHYSTREC
Start date: October 11, 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate the effect of four different follow-up strategies on postoperative recovery following vaginal or abdominal hysterectomy for benign conditions. Furthermore the investigators aim to examine associations between preoperative thresholds for pain (thermal and pressure) and postoperative pain and development of chronic pelvic pain after benign hysterectomy.

NCT ID: NCT01524913 Completed - Pain Clinical Trials

A Double Blind Study Comparing Hyaluronic Acid, Corticosteroid and Placebo During Arthrocentesis for TMJ

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the administration of hyaluronic acid or corticosteroid during arthrocentesis of the temporomandibular joint provides additional pain relief and improved function. The overall hypothesis for the study is that hyalgan will result in a 30% reduction in the mean visual analogue scale (VAS) at one month when compared to celestone and placebo.