Clinical Trials Logo

Pain clinical trials

View clinical trials related to Pain.

Filter by:

NCT ID: NCT01115062 Completed - Pain Clinical Trials

Comparison of Synera Patch Versus LMX-4 Cream Versus Placebo Patch for Pain Reduction During Venipuncture in Children

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effect of Synera patch versus LMX-4 cream and placebo on the level of pain, observed distress, difficulty of venipuncture and skin side effects in children undergoing intravenous blood draw in the emergency setting or the phlebotomy lab.

NCT ID: NCT01111617 Completed - Pain Clinical Trials

Applications of Realtime Functional Magnetic Resonance Imaging (fMRI )

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

The goal of this research program is to determine the potential effectiveness of real-time fMRI training in improving mental control over pain.

NCT ID: NCT01098747 Completed - Pain Clinical Trials

Study Evaluating A Novel Ibuprofen Formulation In The Treatment Of Dental Pain

Start date: April 2010
Phase: Phase 3
Study type: Interventional

This study will compare the pain relieving effect of a single-dose of a novel ibuprofen formulation to placebo and two formulations of standard ibuprofen in the treatment of post-surgical dental pain following "wisdom" tooth (third molar) removal.

NCT ID: NCT01097902 Completed - Pain Clinical Trials

Study of Experimental Models of Pain and Inflammation.

Start date: February 2010
Phase: Phase 1
Study type: Interventional

The experimental pain model studied in this proposal show characteristics of an inflamed wound with a pro-inflammatory response. This study will help discover candidate genetic and/or proteomic pain biomarkers that could provide objective and mechanism based tests to diagnose, monitor or quantify pain. We also hope to determine the measurable effects of a known non-steroidal anti-inflammatory drug (NSAID) on biomarkers of pain and inflammation.

NCT ID: NCT01095900 Completed - Pain Clinical Trials

Comparison of Botulinum Toxin and Sphincterotomy in the Treatment of Chronic Anal Fissure

Start date: n/a
Phase: N/A
Study type: Observational

Intra-sphincteric injection of botulinum toxin seems to be a reliable option causing temporary alleviation of sphincter spasm and allowing the fissure to heal. study is to compare the outcome of surgical sphincterotomy and botulinum toxin injection treatments in patients with uncomplicated chronic anal fissure.

NCT ID: NCT01095575 Completed - Pain Clinical Trials

Pre- Versus Post-Incisional Epidural Morphine: Higher Postoperative Pain Perception and Extra Morphine Consumption

Start date: January 2006
Phase: N/A
Study type: Interventional

Background and Objectives: Neuraxial administration of morphine is an effective way of controlling postoperative pain and reducing analgesic consumption. Several animal models have demonstrated that preemptive administration of neuraxial narcotics reduced pain while others revealed the induction of post-incisional hypersensitivity. There have been no consistent results in clinical setting either. This double blind, randomized study compared the effects of PRE- vs. POST-incisional administration of neuraxial morphine on postoperative pain perception and analgesic requirements over 48 hours following laparotomy for open colectomy under standardized general anesthesia. Methods: Twenty patients received epidural morphine (3 mg) pre-incision and saline after wound closure (MO1 group), and 20 patients received epidural saline before incision and morphine after wound closure (MO2 group). Postoperatively, all patients received boluses of morphine (1.5 mg) via intravenous patient-controlled analgesia (IV-PCA), and rescue doses of intramuscular diclofenac (75 mg) every 6 hours, as needed.

NCT ID: NCT01094925 Completed - Pain Clinical Trials

The Effectiveness of Gabapentin for Post-operative Pain Following Cesarean Section

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

Gabapentin has been very effective at treating pain after knee and hip operations, hysterectomies, and many other types of operations. A previous study at the investigators' hospital found that a single pre-operative dose of 600mg gabapentin produced a significant reduction in pain after caesarean section. However, 19% complained of sedation. The purpose of this study is to see whether a reduced dose of gabapentin will produce a similar improvement in pain scores while avoiding adverse effects such as sedation or dizziness. The objective of this study is to compare the efficacy of a single pre-operative oral dose of gabapentin 300mg, versus 600mg and placebo in women undergoing Cesarean section. The investigators' hypothesis is that gabapentin 300mg will result in decreased pain scores similar to gabapentin 600mg, but with reduced side effects.

NCT ID: NCT01094782 Completed - Pain Clinical Trials

Evaluating the Effect of Acupuncture on Pain Relief Using Quantitative Sensory Testing (QST)

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

The purpose of this study is to explore a new approach in assessing the effectiveness of acupuncture therapy in the treatment chronic pain conditions.

NCT ID: NCT01094522 Completed - Pain Clinical Trials

Measuring the Amount of Methadone or Morphine in the Blood of Neonates, Infants & Children After Cardiac Surgery.

Start date: March 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Study Population: Neonates, infants and children from birth to 5 years of age undergoing cardiac surgery with CPB. The use of methadone to provide analgesia may be increasing due to advantages compared to other commonly used opioid analgesic drugs. While efficacy of methadone has been reported in adults, there is a paucity of information in neonates and infants. In the latter population, fentanyl and morphine are most commonly used for opioid analgesia following major surgery, while methadone is frequently used for weaning of opioid dependent and tolerant patients, in spite of the paucity of knowledge of methadone pharmacology in this population. There are several clinical problems associated with fentanyl and morphine, and methadone may offer superior efficacy with fewer side effects than these agents. We propose to study the pharmacokinetics (PK) and pharmacodynamics (PD) of methadone in neonates and infants in the intensive care unit following cardiac surgery.

NCT ID: NCT01094366 Completed - Pain Clinical Trials

Paracervical Block for Pain Control in First Trimester Abortion

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

Many woman undergoing a surgical abortion receive a paracervical nerve block for pain reduction, in which lidocaine (a numbing medication) is injected around the cervix. These injections numb the cervix and possibly the lower part of the uterus. However, the injection can be uncomfortable and it is not well known whether it is effective in reducing pain. The purpose of this study is to determine the level of pain women experience with a surgical abortion and the effect that paracervical block might have on that pain.