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Pain clinical trials

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NCT ID: NCT03397082 Completed - Pain Clinical Trials

Topic Cervical Anesthesia for Pain Control During Endouterine Manual Aspiration

Start date: August 1, 2014
Phase: N/A
Study type: Interventional

To compare the effectiveness of lidocaine gel plus paracervical blockade vs. Paracervical blockade alone in the management of pain during endouterine manual aspiration.

NCT ID: NCT03396250 Completed - Pain Clinical Trials

A Pharmacokinetic Trial of Naproxen Sodium and Diphenhydramine Hydrochloride Soft Capsules Versus Naproxen Sodium and Diphenhydramine Hydrochloride Tablets in Healthy Adult Subjects

Start date: February 12, 2018
Phase: Phase 1
Study type: Interventional

To evaluate the relative bioavailability of Naproxen Sodium 220 mg and diphenhydramine hydrochloride (DPH HCL) 25 mg soft capsules (Test) versus Naproxen Sodium 220 mg and diphenhydramine hydrochloride 25 mg tablets (Reference) after a single oral administration under fasted condition in healthy adults subjects. To assess the safety and tolerability of the investigational products in terms of advent events (AEs) and clinical parameters.

NCT ID: NCT03394807 Completed - Pain Clinical Trials

LaGRA Trial in Laparoscopic Cholecystectomy

LaGRA
Start date: October 1, 2016
Phase: Phase 4
Study type: Interventional

This study investigated the effectiveness of a surgeon administered, laparoscopic guided, regional anaesthesia technique.

NCT ID: NCT03393910 Completed - Pain Clinical Trials

The Improvement Of Pelvic Exams for Patients With Chronic Vulvovaginal Conditions

Start date: January 22, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate patients self-reported comfort levels during each section of the pelvic exam.

NCT ID: NCT03393533 Completed - Pain Clinical Trials

Evaluation of the Effectiveness of the Use of the Therapeutic Bandage Method in Third Molar Surgery

Start date: October 20, 2017
Phase: N/A
Study type: Interventional

Extraction of lower third molars semi-included or included is one of the most performed procedures in oral surgery, and inherent to the procedure there is a postoperative inflammatory response. Among the factors most routine to this response are pain, edema and trismus. The therapy taping has advantages in its use in the physiotherapy of several specialities, leading to the correction of muscular functions, reduction of edema, muscular spasms and reduction of pain. Thus, the objective of this split mouth, randomized, blind, clinical trial will be to evaluate the postoperative period of 32 third molars in the patients from the São Paulo State University (Unesp), Institute of Science and Technology, São José dos Campos, Brasil. These evaluations will be performed on the third and seventh days after the extraction, where the patients will be analyzed by evaluator who will measure the edema, the opening of the mouth (evaluation of muscle spasm) and collect the pain table delivered in the immediate postoperative period, comparing thus, the benefit of therapeutic banding in the postoperative period of the extraction of lower third molars. The analogue pain scale (VAS), together with the Ustün et al. (2003) and the millimeter rule will be used to compare the data and the results will be submitted to descriptive statistics and compared by means of the statistical analysis of variance (ANOVA) and Tukey test with significance level of 5%.

NCT ID: NCT03384160 Completed - Pain Clinical Trials

Evaluation of Articaine 4% Versus Mepivacaine 2% for Surgery of Molars Thirds: Clinical Trial.

Start date: December 7, 2017
Phase: N/A
Study type: Interventional

The extraction of third molars, a frequent treatment in clinical dental practice, can lead patients to painful symptoms during and after surgery. The dental surgeon must correctly indicate the need for extraction and also provide patients who need this treatment greater comfort and control of pain in the trans and postoperative period. Thus, it is necessary to use an effective local anesthetic favoring the factors inherent to the postoperative and achieving good treatment results.

NCT ID: NCT03380949 Completed - Pain Clinical Trials

Monitor-Guided Analgesia During General Anesthesia - Part II

MOGADA-II
Start date: December 8, 2017
Phase: N/A
Study type: Interventional

This prospective randomized clinical trial evaluates the effects of a monitor-guided opioid analgesia during general anesthesia. To date no standard-monitoring device exists to specifically reflect the analgesic component of general anesthesia. Quality and safety of general anesthesia are of major clinical importance and should be improved by limiting the opioid analgesic's dosage to the minimum amount needed. The study compares the effects of monitoring nociception during general anesthesia with different innovative techniques in comparison to routine clinical practice.

NCT ID: NCT03380247 Completed - Pain Clinical Trials

Multimodal Oral Analgesia for Trauma in the Emergency Department

START
Start date: October 12, 2017
Phase:
Study type: Observational

The prevalence of pain in the emergency department is estimated between 60% and 78%. However, many studies reported oligo analgesia in about half of patient admitted to the emergency department. The delay before effective analgesia is one of the main causes of oligoanalgesia. The use of nurse-directed protocol allows the administration of analgesic upon admission to the emergency department. Nevertheless the need of intravenous access may delay analgesia. The use of oral form analgesics even with immediate release does not allow effective analgesia before 20 min. Pain management protocol in the emergency reception desk of CHU Grenoble Alpes (CHUGA) includes paracetamol that can be combined with oxycodone tablets depending on the pain intensity. For any mono traumatized it is possible to associate self-administer methoxyflurane inhaler. The pain management protocol is already used in the emergency reception desk of CHU Grenoble Alpes.The different analgesics( paracetamol,oral oxycodone, methoxyflurane) are already administered as part of routine care.The use of these different analgesics means would allow a rapid and adapted effectiveness to the pain intensity. However, there are no data on the efficacy and acceptability of such an early multimodal analgesia protocol in the emergency department.

NCT ID: NCT03377907 Completed - Pain Clinical Trials

Pain Alleviation of Forearm Fractures

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

fractures of upper limb induce much pain . A lot of modalities are available to alleviate pain. fracture hematoma block, and intravenous regional anesthesia seem to be cost effective and attractive options

NCT ID: NCT03377816 Completed - Pain Clinical Trials

The Role of Emotional Processing in Improving the Quality of Life of Breast Cancer Patients

REPAT
Start date: June 11, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to examine two mechanistic changes: emotion processing (awareness, expression and acceptance) and cholinergic anti-inflammatory processes (HRV and cytokine expression) through which an Art Therapy (AT) intervention reduces depression, pain and fatigue.