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Acute Pain clinical trials

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NCT ID: NCT03699280 Completed - Acute Pain Clinical Trials

Virtual Reality and Outpatient Hysteroscopy

VISTA
Start date: August 4, 2018
Phase: N/A
Study type: Interventional

TITLE Virtual Reality (VR) as a Distraction technique for management of acute pain at Outpatient Hysteroscopy DESIGN Randomised Control Trial (RCT) with Mixed methods - Qualitative and quantitative AIMS To study the role of distraction techniques for management of acute pain in Outpatient Hysteroscopy and to assess feasibility of using Virtual Reality for managing pain. Primary objective: • Feasibility of using virtual reality as a distraction technique in management of acute pain in patients undergoing Outpatient Hysteroscopy. Secondary objectives: - Understanding the acceptability and effectiveness of VR interventions within the procedural groups and how these might vary as a function of different patient demographics. - Understanding the factors that might influence the willingness of patients to participate in a future formal trial of the technology. - Understanding how best to implement the technology and designing of the contents of the VR intervention. - Understanding the effective mechanisms for the analgesic effect of VR and explore how this could be tailored to individual patients. POPULATION Patients attending the Outpatient Hysteroscopy clinics ELIGIBILITY Patients undergoing Outpatient Hysteroscopy DURATION 6 months

NCT ID: NCT03693820 Completed - Pain, Acute Clinical Trials

Gall Bladder Bed Infiltration Analgesia

Start date: September 10, 2018
Phase: N/A
Study type: Interventional

Early postoperative pain is a common complaint after elective laparoscopic cholecystectomy. Persistent acute postoperative pain is the dominating complaint and the primary reason for a prolonged stay after this procedure. This pain can be superficial incisional wound pain (somatic), deep visceral pain and/or post-laparoscopy shoulder pain (referred somatic), all of which may require systemic analgesia. Hypothesis: Laparoscopic pain can be superficial incisional wound pain (somatic pain), deep visceral pain and/or post-laparoscopy shoulder pain (referred somatic pain), so the block must be periportal for incisional wound pain, intraperitoneal to decrease pain caused by pneumoperitoneum, and of the bladder bed to decrease the deep visceral pain. This combination can give the maximum analgesia after laparoscopic cholecystectomy.

NCT ID: NCT03672162 Completed - Clinical trials for Total Abdominal Hysterectomy ,Pain , Acute Postoperative,Gabapentin , Celecoxib

Preoperative Analgesia in Non-gynecological Cancerous Women Who Underwent Elective Total Abdominal Hysterectomy

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

Comparison of effectiveness of preoperative Gabapentin with Celecoxib in reducing acute postoperative pain in abdominal hysterectomy, A randomized double blind controlled trial

NCT ID: NCT03665727 Completed - Acute Pain Clinical Trials

Psychosocial Support for Pre-operative Pain and Distress

Mind-Body JRA
Start date: June 4, 2018
Phase: N/A
Study type: Interventional

The purpose of this randomized study is to determine the impact of three different types of psychosocial support delivered by mental health professionals to pre-operative joint replacement patients. This study will examine the differential effects of brief mindfulness training, hypnostic suggestion, and cognitive behavioral pain psychoeducation for pre-operative patients, with a supplemental nonrandomized usual care comparison group.

NCT ID: NCT03664622 Completed - Acute Pain Clinical Trials

Ketamine Versus Morphine Change Pain Profile

Start date: September 15, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the efficacy of intravenous low dose ketamine infusion versus morphine infusion analgesia for pain reduction in Abdominoplasty surgery

NCT ID: NCT03662152 Completed - Pain, Acute Clinical Trials

Effects of Vibration Foam Rolling After Muscle Damage

Start date: January 7, 2018
Phase: N/A
Study type: Interventional

Purpose: To compare the effects between non-vibration foam rolling (NVFR) and vibration foam rolling (VFR) on visual analogic scale (VAS), pressure pain threshold (PPT), oxygen saturation (SmO2), counter-movement jump (CMJ), and hip and knee range of movement (ROM) after induction of muscle damage through eccentric acute-exercise using inertial flywheel. Methods: Thirty-eight healthy subjects (males n=32 females= 6, age 22.2±3.2 years) were randomly assigned in a counter-balanced fashion to either a VFR or NVFR protocol group. All subjects performed a 10x10 (sets x reps) eccentric squat protocol to induce muscle damage. The protocols were administered 48-h post-exercise, measuring VAS, PPT, SmO2, CMJ and ROM, before and immediately post-treatment. The technique of treatment was repeated on both legs for 1 min for a total of 5 sets, with a 30-s rest between sets.

NCT ID: NCT03657810 Completed - Pain Clinical Trials

A Controlled Study to Determine the Efficacy and Safety of CL-108 5 mg for Acute Pain and the Prevention of OINV

Start date: August 2, 2017
Phase: Phase 3
Study type: Interventional

To determine the analgesic efficacy of CL-108 5 mg by comparison with placebo and the anti-emetic efficacy of CL-108 5 mg by comparison with hydrocodone 5 mg/acetaminophen 325 mg.

NCT ID: NCT03653260 Completed - Pain, Acute Clinical Trials

A Study to Evaluate the Efficacy and Safety of Zingo in Chinese Children

Start date: August 15, 2018
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy and safety of Zingo in treating pain associated with venipunture and peripheral venous cannulation.

NCT ID: NCT03647683 Completed - Acute Pain Clinical Trials

Self-Compassion and Acute Pain

Start date: April 15, 2018
Phase: N/A
Study type: Interventional

Research on self-compassion suggests its impact in the context of pain. In the current study, the investigators evaluate a short self-compassion intervention for coping with acute pain.

NCT ID: NCT03641911 Completed - Pain, Acute Clinical Trials

Incidence of Inadequate Pain Treatment in Ventilated Critically Ill Surgical Patients

Start date: November 15, 2017
Phase:
Study type: Observational

In SICU, Siriraj hospital there were no protocols place for the management of pain. All decisions were made according the attending physicians. There were no information about incidence of inappropriate pain management in SICU due to lack of validated tool for assessment. To date, Thai-version of BPS and CPOT were validated, the incidence of inappropriate pain management in SICU, Siriraj hospital should be assessed.