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Pain clinical trials

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NCT ID: NCT00855803 Completed - Pain Clinical Trials

Stereotactic Body Radiation Therapy and Vertebroplasty in Treating Patients With Localized Spinal Metastasis

Start date: February 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: Stereotactic body radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue. Vertebroplasty may help prevent fractures and spinal cord compression caused by spinal metastasis. Giving stereotactic body radiation therapy together with vertebroplasty may help lessen pain and improve quality of life of patients with spinal metastasis. PURPOSE: This phase II trial is studying how well giving stereotactic body radiation therapy together with vertebroplasty works in treating patients with localized spinal metastasis.

NCT ID: NCT00853970 Completed - Pain Clinical Trials

Efficacy Study of Bromfenac Ophthalmic Solution in Patients Undergoing Cataract Surgery

Start date: February 2009
Phase: Phase 3
Study type: Interventional

Efficacy study of Bromfenac Ophthalmic Solution in cataract surgery

NCT ID: NCT00853333 Completed - Pain Clinical Trials

Sedation and Pain (The Effect of IV Sedation on Pain Perception)

Start date: November 2008
Phase: N/A
Study type: Interventional

The investigators propose to evaluate the potential effect of sedation on pain perception in two ways, by asking for a participant's pain rating(subjective) and by evaluating a subject's brain activation using fMRI(objective).

NCT ID: NCT00853177 Completed - Pain Clinical Trials

MEOPA Breathing Analgesia for Oocyte Retrieval(KALOVAL)

KALOVAL
Start date: November 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess pain, at or after oocyte retrieval, the effectiveness of self-controlled inhalation analgesia by nitrous oxide (N2O of 50% and 50% O2) by the patient compared to a local anesthesia combined with a tablet of 0.5 mg of Alprazolam.

NCT ID: NCT00852917 Completed - Pain Clinical Trials

A Four-Arm Study Comparing the Analgesic Efficacy and Safety of Tramadol Once a Day 100, 200 and 300 mg Versus Placebo for the Treatment of Pain Due to Osteoarthritis of the Knee (With 7-Day Follow-up)

Start date: January 2003
Phase: Phase 3
Study type: Interventional

The objective of this study is to compare the analgesic efficacy and safety of Tramadol Once a Day 100, 200, 300 mg and Placebo

NCT ID: NCT00852865 Completed - Pain Clinical Trials

Lactobacillus Farciminis and Hyperalgesia

Start date: February 2009
Phase: Phase 1
Study type: Interventional

We want to analyse a possible effect of o dialy consumption of Lactobacillus farciminis on a hyperalgesia on response to thermal stimulation. A comparaison of results before and after three weeks of treatment will be made.

NCT ID: NCT00847418 Completed - Pain Clinical Trials

Pharmacokinetics and Pharmacodynamics of Nasally Applied Esketamine

Start date: February 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is the determination of blood concentration and the effectiveness of esketamine after nasal application.

NCT ID: NCT00845754 Completed - Pain Clinical Trials

Post-Operative Treatment With Ketorolac After Abdominal Myomectomy

Start date: September 1999
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if ketorolac, given after abdominal myomectomy, will decrease the frequency of post-oerative fevers as well as improve post-operative pain management.

NCT ID: NCT00836316 Completed - Pain Clinical Trials

Levobupivacaine During Cholecystectomy

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effects of intraperitoneal administration of levobupivacaine on pain after laparoscopic cholecystectomy.

NCT ID: NCT00836134 Completed - Pain Clinical Trials

Ultrasound-guided Rectus Sheath Block for Post-operative Pain Control Following Umbilical Hernia Repair

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

The purpose of this study is to compare the effectiveness of local infiltration to an ultrasound guided nerve block placed by the anesthesiologist for children undergoing umbilical hernia repair. This is a double-cohort, double blinded, randomized study comparing local infiltration to ultrasound-guided rectus sheath block in children 1 to 17 years of age undergoing epigastric or umbilical hernia repair. We will first compare pain scores to see if one method is more adequate then the other in providing post-op analgesia. Our second aim is to compare morphine consumption between the two groups. Our third aim is to measure the levels of local anesthetic in the blood following local anesthetic infiltration or USGRSB.