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Pain clinical trials

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NCT ID: NCT00803114 Completed - Pain Clinical Trials

Epidural Morphine Following Vaginal Delivery

Start date: March 2002
Phase: Phase 4
Study type: Interventional

The investigators believe that pain management following a vaginal delivery can be improved. Many women receive epidural medication during labor and delivery, and the investigators felt that using the epidural following delivery might improve the first day pain. This study is to determine whether a single dose of epidural morphine given to mothers after a vaginal delivery will reduce the perineal pain in the postpartum period.

NCT ID: NCT00802308 Completed - Pain Clinical Trials

Effects of a Single Dose of Egalet® Morphine Combined With a Single Dose of Alcohol in Healthy Moderate Drinkers

Start date: December 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the pharmacokinetics of Egalet® morphine when administered with alcohol and compare to administration with water.

NCT ID: NCT00802087 Completed - Pain Clinical Trials

Single Dose Pharmacokinetics of Egalet® Hydrocodone

Start date: November 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the pharmacokinetic profile of different Egalet® hydrocodone formulations and compare to a marketed hydrocodone drug.

NCT ID: NCT00801983 Completed - Pain Clinical Trials

The Effect of Alternative Keyboards on Discomfort and Typing Kinematics

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

Awkward postures during computer keyboard use have been hypothesized to be one cause of musculoskeletal pain/discomfort as well as musculoskeletal disorders of the upper extremity (MSD-UE). Alternative computer keyboards purport to reduce musculoskeletal pain/discomfort and have been shown to change aspects of keyboard users' kinematics under laboratory conditions. However, research that has examined the effectiveness of alternative keyboards in reducing musculoskeletal pain/discomfort in the workplace is equivocal, and no study has examined the association between postures and musculoskeletal pain. The Aims of this 3-year prospective double cross-over trial are: 1) To examine the effectiveness of an alternative keyboard in reducing reports of pain over 6-months; 2) To examine the neutrality and stability of postures during keyboard use; and 3) To identify which postures are associated with lower levels of musculoskeletal pain. Seventy-five computer users will be randomly assigned to one of two keyboard use orders: Group 1 - AB (standard keyboard, alternative keyboard); Group 2 - BA (alternative keyboard, standard keyboard). All subjects will use their assigned keyboards for 6-months before switching to the next keyboard. Every week, subjects will report their musculoskeletal pain levels. Just prior to and just after each 6-month intervention subjects' kinematics performances on the keyboards will be recorded at the worksite using the Keyboard - Personal Computing Style (K-PeCS) instrument and in a laboratory setting using 3-dimensional motion capture technology. Aim 1: To examine the effectiveness of an alternative keyboard in reducing pain over 6-months. Hypothesis 1 (H-1) - At six months subjects using an alternative keyboard will have significantly lower musculoskeletal pain levels than when using a standard keyboard. Aim 2: To examine the neutrality and stability of postures during keyboard use. Hypothesis 3 (H-2) - Subjects using an alternative keyboard will have significantly more neutral postures than when using a standard keyboard at baseline and at 6 months Hypothesis 3 (H-3) - Subjects 6-months keyboarding postures will remain equivalent to the keyboarding postures documented at baseline.

NCT ID: NCT00801788 Completed - Pain Clinical Trials

Single Dose Pharmacokinetics of Egalet® Oxycodone

Start date: September 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the pharmacokinetic profile of different Egalet® oxycodone formulations and compare to a marketed oxycodone product.

NCT ID: NCT00801047 Completed - Pain Clinical Trials

Intravenous Remifentanil Patient-controlled Analgesia (PCA) and Epidural Patient Controlled Epidural Analgesia (PCEA) for Labor Analgesia

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

Women requesting analgesia do not always wish to receive a potent analgesic method, and may fear the risks of epidural analgesia. Study Aim: To determine whether remifentanil is effective for labor analgesia when compared with standard treatment (epidural analgesia).

NCT ID: NCT00799656 Completed - Pain Clinical Trials

Efficacy and Safety Study of Ataciguat Versus Placebo in Patients With Neuropathic Pain

SERENEATI
Start date: November 2008
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the efficacy of ataciguat versus placebo in reducing pain intensity in patients with neuropathic pain. The secondary objective is to assess the safety and tolerability of ataciguat versus placebo.

NCT ID: NCT00798941 Completed - Pain Clinical Trials

ICU Patient and Family Comfort Study

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

The purpose of this study is to evaluate family-led interventions for Intensive Care Unit (ICU) patients' symptoms (i.e., pain and thirst) that will involve ICU patients' family members in the non-pharmacological management of these symptoms. This family involvement may help to ameliorate not only patients' symptoms but also the families' symptoms and promote family satisfaction with ICU care.

NCT ID: NCT00793286 Completed - Pain Clinical Trials

Stapler Versus Glue for Laparoscopic Groin Hernia Repair

Start date: August 2004
Phase: N/A
Study type: Interventional

Repair of inguinal hernia is the most common operation of the general surgeon. In recent years, it was recognized that chronic postoperative pain is as important for postoperative outcome as recurrent hernia. The incidence of pain or discomfort ranges up to 60% of operated patients. Despite the fact that laparoscopic hernia repair has been shown to reduce postoperative pain compared to open hernia repair, up to 5% of patients suffer from persistent discomfort. During that operation the mesh is either fixed using a stapler or tissue adhesive glue. With the current study we compare postoperative pain between patients undergoing laparoscopic inguinal hernia repair with either mesh fixation using a stapler or tissue adhesive. The use of von Frey monofilaments allows to describe pain with a high sensitivity.

NCT ID: NCT00793117 Completed - Pain Clinical Trials

The Effect of Packing in Post Operative Management of FESS

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

Chronic sinusitis is a very common problem. The functional endoscopic sinus surgery is a prevalent option to treat this disease.During usage of different techniques of surgery, the need for packing after surgery is debatable problem. So to solve this problem this research has been designed.