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Pain, Acute clinical trials

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NCT ID: NCT06191770 Completed - Pain, Acute Clinical Trials

Comparison of Morphine With Nalbuphine in a Multimodal Approach for Pain Relief in Patients Undergoing Gynecological Procedures: Randomized Controlled Double Blind Clinical Trial

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

This study was conducted in the Aga Khan University Hospital, Karachi. Pakistan is developing country and overall shortage of Morphine in developing country. Rationalizing, in multimodal analgesia, Nalbuphine is equivalent to morphine in open Abdominal hysterectomy

NCT ID: NCT06131606 Completed - Pain, Acute Clinical Trials

Effect of Stress Ball in Angiography

Start date: January 10, 2023
Phase: N/A
Study type: Interventional

The target of this study was to determine the influence of stress ball application on pain and anxiety levels experienced by patients during angiography procedures.

NCT ID: NCT06131593 Completed - Pain, Acute Clinical Trials

TAP Block With Methyl-prednisolone as a Pain Treatment Modality After Total Abdominal Hysterectomy Procedures

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

The aim of this work to compare between the efficacy of ultrasound guided TAP block with dexamethasone as an adjuvant versus ultrasound guided TAPB with methyl prednisolone as an adjuvant to local anesthetic for postoperative pain management in lower abdominal hysterectomy procedures.

NCT ID: NCT06130384 Completed - Pain Clinical Trials

Pain Reduction With Topical Bromfenac Versus Artificial Tear After Intravitreal Injection.

Start date: March 1, 2021
Phase: Phase 4
Study type: Interventional

The purpose of this prospective interventional study is to compare post-intravitreal injection pain between eyes receiving topical bromfenac versus artificial tears as an analgesic after intravitreal injection.

NCT ID: NCT06125613 Completed - Pain, Acute Clinical Trials

Influence of Kinesiophobia on the Excitability of Connections Parieto-frontal During a Pointing Movement in Humans

pIPS/M1
Start date: December 10, 2021
Phase: N/A
Study type: Interventional

Objective(s) of the trial: Better understand the interaction between kinesiophobia and motor control. Main objective: To measure the influence of induced kinesiophobia on functional connectivity between the posterior parieto-occipital region and the primary motor cortex in healthy subjects during a pointing task. Secondary objectives: The secondary objectives will be 1) to verify the excitatory influence of pIPS stimulation on the excitability of M1 at rest and 2) to establish whether there is a correlation between functional connectivity and the level of kinesiophobia ( as measured by the Tampa Scale)

NCT ID: NCT06113926 Completed - Pain, Acute Clinical Trials

Racial Discrimination, Pain, and the Buffering Influences of Acknowledgment

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

Black young adults (aged 18-30; N = 92) were racially included (i.e., received the ball an equal number of times) or excluded (i.e., received the ball only once) by other White players in a ball-tossing computer game called Cyberball; White experimenters acknowledged the exclusion for half of the excluded participants. Participants completed a cold-pressor task twice to measure pain sensitivity (threshold, tolerance, and unpleasantness): immediately prior, and after the Cyberball (and acknowledgment) manipulation. Participants also completed a post-manipulation survey examining the psychological effects of racial exclusion and acknowledgment (i.e., psychological needs satisfaction, negative affect, control).

NCT ID: NCT06086106 Completed - Pain, Postoperative Clinical Trials

Comparison Between the Caudal Block and Other Methods of Postoperative Pain Relief in Children Undergoing Circumcision

paincontrol
Start date: May 1, 2023
Phase:
Study type: Observational

Prospective, randomized, case-controlled trial study. Observation post-operatively: Aims: This study aimed to compare the effectiveness of the caudal block CB with other methods of postoperative pain release.

NCT ID: NCT06072950 Completed - Pain Clinical Trials

Opioid Use and Predicting Factors at the Emergency Department

VRxOPUS-1
Start date: February 13, 2023
Phase:
Study type: Observational

Background: Increasing opioid misuse is a worldwide problem. About 10% of opioid misusers are primarily exposed to opioids at the Emergency Department (ED). This study was conducted to determine the feasibility for a clinical trial investigating the effect of Virtual Reality therapy on opioid consumption at the ED. Methods: Adult patients were included when primarily seen by the Emergency Physician and presenting with a NRS pain score ≥4. Main objective was to identify the target population and evaluate outcome measures to sustain a trial incorporating the Oral Morphine Equivalent (OME) at the ED as the primary endpoint. Primary outcome was mean OME administered at the ED. Secondary outcomes included NRS pain scores, main symptoms and type of analgesics administered at the ED.

NCT ID: NCT06011668 Completed - Pain, Acute Clinical Trials

EFFECT OF DISTRACTION METHODS ON PAIN AND ANXIETY DURING INTRAMUSCULAR INJECTION IN CHILDREN

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

This thesis study was conducted in an unblinded, randomized controlled experimental manner in order to analyze the effect of attention-drawing methods that can be used during intramuscular injection in children on pain and anxiety.

NCT ID: NCT06005480 Completed - Healthy Clinical Trials

Understanding Rebound Pain After Regional Anesthesia Resolution in Healthy Volunteers

Start date: September 28, 2023
Phase: Phase 1
Study type: Interventional

Regional anesthesia decreases postoperative pain scores and opioid consumption, and may prevent chronic pain after surgery in patients undergoing surgery. However, some patients experience an increase of pain into the severe range when the nerve block wears off, also known as rebound pain. The investigators are studying if a nerve block (numbing injection) in the arm causes hyperalgesia (increased pain) when the nerve block is wearing off.