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Pain clinical trials

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NCT ID: NCT01406756 Recruiting - Pain Clinical Trials

Combination Chemotherapy in Treating Young Patients With Newly Diagnosed High-Risk Acute Lymphoblastic Leukemia

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

This randomized phase III trial is studying how well combination chemotherapy works in treating young patients with newly diagnosed acute lymphoblastic leukemia that is likely to come back or spread. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) and giving the drugs in different doses and in different combinations may kill more cancer cells.

NCT ID: NCT01375283 Recruiting - Pain Clinical Trials

Sensory Mapping Following Video-assisted Thoracic Surgery

Start date: June 2011
Phase: N/A
Study type: Observational

This is a prospective observational cohort study on changes in sensory mapping.

NCT ID: NCT01329874 Recruiting - Pain Clinical Trials

Anesthetic Efficacy of Gow-Gates Versus Conventional Inferior Alveolar Nerve Block Techniques

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

The purpose of this study is to determine whether Gow Gates block injection is more effective than conventional alveolar nerve block in anesthetising mandibular molars with acute pulpitis.

NCT ID: NCT01312259 Recruiting - Sexual Dysfunction Clinical Trials

Clinical Efficacy of Changing the InterStim® Parameters in Patients With Interstitial Cystitis/Painful Bladder Syndrome

Start date: April 2011
Phase: Phase 4
Study type: Interventional

Purpose: 1. To demonstrate better symptoms control (pain, urinary urgency and frequency) with sacral neuromodulation (SNM) in patients with interstitial cystitis /painful bladder syndrome (IC/PBS) using a stimulation frequency of 40 hertz (experimental) compared to a frequency of 14 hertz (standard). 2. The evaluate the efficacy of the two frequency settings on the other associated conditions that often coexist in patients with IC/PBS, such as female sexual dysfunction (FSD), bowel dysfunction, high tone pelvic floor dysfunction (HTPFD, painful spasm of the pelvic floor muscles), Vulvodynia (pain at the opening of the vagina).

NCT ID: NCT01285284 Recruiting - Pain Clinical Trials

Effect of Music Over the Tolerance to Colonoscopy.

EMOC
Start date: March 2011
Phase: Phase 4
Study type: Interventional

This study will evaluate the efficacy of music (a very well selected list of songs)on improving the tolerance to the colonoscopy. The patients will be randomly assigned to receive music or not. The authors hypothesis is that music is able to improve the tolerance to colonoscopy evaluated as a reduction on the level of anxiety, on the intensity of pain experimented during the procedure and a reduction of the administered dose of midazolam during the colonoscopy.

NCT ID: NCT01246323 Recruiting - Pain Clinical Trials

Combined Anesthesia for Laparoscopy Surgery in Gynecology

Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether combined anesthesia will provide better pain control for the postoperative period following gynecological laparoscopy surgery.

NCT ID: NCT01230463 Recruiting - Pain Clinical Trials

Study of Whether 15 mg Dose of Ketorolac IV is as Effective as a 30 mg Dose.

Start date: September 2010
Phase: N/A
Study type: Interventional

The primary aim of this study is to show the non-inferiority of 15 mg intraoperative dose of ketorolac as compared to the standard 30 mg ketorolac by looking at the VAS scores 4 hours after an adult spine surgery.

NCT ID: NCT01207206 Recruiting - Pain Clinical Trials

Oral Ketamine as an Adjuvant to Opioids for Pain Treatment in Cancer Patients

Start date: October 2010
Phase: N/A
Study type: Interventional

In the current research the investigators would like to examine the effect of a well acquainted drug, Ketamine, which is used by anesthesiologists to induce sleep in operations. Usually the ketamine is given into the vein and not orally. The investigators want to give it orally to cancer patients that sufffer from severe pain to find out whether it can prove their quality of life, lower their pain and reduce the amount of opioids they receive.

NCT ID: NCT01119911 Recruiting - Pain Clinical Trials

Blood Sampling Through Peripheral Venous Catheter in Infants

Start date: May 2010
Phase: N/A
Study type: Observational

We hypothesize that peripheral venous catheter used for fluid administration can replace venipuncture blood sampling for selected basic analytes and thus reduce pain in infants under 2 years of age.

NCT ID: NCT01080911 Recruiting - Pain Clinical Trials

0.05 mg Versus 0.1 mg Spinal Morphine for Reducing Morphine Requirement After Vaginal Hysterectomy

Start date: March 2010
Phase: Phase 4
Study type: Interventional

This study aims to compare the effect of spinal morphine between the dose 0.05 mg and 0.1 mg on the amount of morphine during the first 24 hours postoperative.