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Pain clinical trials

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NCT ID: NCT04556747 Completed - Pain Clinical Trials

FOREVR Peds VR Pilot

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

To determine the feasibility and acceptability of using immersive virtual reality technologies to impact clinical outcomes (e.g., pain and anxiety) and medication utilization (e.g., narcotics) in pediatric patients with acute and chronic pain.

NCT ID: NCT04545229 Completed - Pain Clinical Trials

VR for Pain Management During Adult Burn Dressing Change

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

A randomized controlled trial to evaluate the efficacy of the VR-based Pain Alleviation Tool (VR-PAT) in reducing opioid pain medication use during adult burn dressing changes.

NCT ID: NCT04544631 Completed - Pain Clinical Trials

VR for Pediatric Burn Dressing Changes

Start date: December 1, 2016
Phase: N/A
Study type: Interventional

This study evaluated a smart phone virtual reality (VR) to manage pediatric burn dressing pain. A randomized controlled trial was conducted among 90 patients (6-17 years). Active VR participants played the game, passive VR group were immersed in the same VR without interactions, and a standard care group served as the control. One researcher administered VR and observed pain while another researcher administered post-trial survey that measured child's perceived pain and VR experience. Nurses were asked to report the clinical utility.

NCT ID: NCT04543435 Completed - Pain Clinical Trials

Investigation of Pain Coping Methods and Related Factors in Postmenopausal Women

Start date: September 17, 2020
Phase:
Study type: Observational

Musculoskeletal pain (MSP) reflects of musculoskeletal conditions related to tissues such as tendons, muscles, ligaments, nerves, and other joint structures. Coping strategies with pain are used to manage the pain and its impacts. The present study aimed to compare active and passive coping strategies used and pain severity in postmenopausal women according to their demographic characteristics. Also, the relationship between pain and coping strategies in postmenopausal women with cMSP will be examined.

NCT ID: NCT04543227 Completed - Pain Clinical Trials

Opioid Laws and Pediatric Use

Start date: September 10, 2020
Phase:
Study type: Observational

The legitimate need for opioid medications for acute pain management in pediatric trauma patients is recognized, however, the high dose and duration of opioid drugs prescribed by medical providers has been associated with an increased risk of opioid abuse and chronic use by patients. The overarching goal of application is to assess opioid use and outcomes of pediatric patients treated for either burn injuries or knee arthroscopy procedures at a large academic pediatric medical center before and after Ohio opioid prescription rules for acute pain were implemented on August 21, 2017. Also, to evaluate patient use of opioids at 90-days post-treatment.

NCT ID: NCT04526132 Completed - Pain Clinical Trials

A Phase Ⅲ Clinical Study Trial of Felbinac Trometamol Injection in China

Start date: April 25, 2021
Phase: Phase 3
Study type: Interventional

A multi-center, randomized, double-blind, placebo parallel controlled phase Ⅲ clinical trial on the efficacy and safety of felbinac trometamol Injection in the treatment of moderate and severe postoperative pain.main purpose is to evaluate the efficacy of Felbinac Trometamol Injection in the treatment of moderate and severe pain after surgery.Secondary purpose is to evaluation the safety of Felbinac Trometamol Injection in the treatment of moderate and severe pain after surgery.

NCT ID: NCT04523935 Completed - Pain Clinical Trials

Excessive Crying in Children With Cerebral Palsy and Communication Deficits

ECCCPCD
Start date: December 7, 2005
Phase: Phase 4
Study type: Interventional

Management of excessive crying in children with cerebral palsy and communication deficits [ECCCPCD] was guided by the associated clinical findings and investigations.

NCT ID: NCT04520958 Completed - Pain Clinical Trials

Preoperative Psychosocial Support for Postoperative Recovery and Health: Mechanistic Substudy

Start date: October 29, 2019
Phase: N/A
Study type: Interventional

This was a single site, three-arm, parallel group randomized clinical trial that compared the effect of three preoperative psychosocial interventions on knee and hip replacement patients' preoperative pain intensity and postoperative pain intensity, pain unpleasantness, and opioid use.

NCT ID: NCT04512651 Completed - Pain Clinical Trials

The Thrust Technique of Tibiotarsal Joint on the Symptomatology of Pain at Classical Ballet Dancers

Start date: June 10, 2017
Phase: N/A
Study type: Interventional

Classical ballet is a type of high performance dance that requires great effort and extreme joint positions by its dancers, not to mention a precise control of the ankle joint when on pointe position. Ballet dancers excessively dorsiflex, and especially plantar flex the ankle, which predisposes anterior displacement of the talus, possibly causing mobility restrictions of the tibiotarsal articulation and making it difficult and painful to move the ankle while dancing. The Thrust technique of tibiotarsal joint is a manipulation that aim to improve mobility and articular function through a high-speed and short-range movement. The purpose of the study is to verify the effect of the Thrust technique of tibiotarsal joint on the pain symptomatology in classical ballet dancers. Ballerinas included in the study presented pain in the ankle when dancing classical ballet, tenderness to palpation in the anterior and posterior tibiotarsal articulation, and dysfunction after compression of the tibiotarsal articulation. The sample consisted of 20 ballerinas, out of which 10 were subjected to manipulation (IG) and 10 formed the control group (CG). Algic symptomatology in classical ballet dance was assessed after some practice with the Visual Analogue Scale (VAS). After that, an algometer was used to quantify the threshold of pain in the anterior and posterior ankle joint that presented restrictions in mobility. The Tug technique was performed in the tibiotarsal articulation in the IG, and in the CG it was simulated. The threshold of pain in the anterior and posterior tibiotalar joint was measured again immediately after the intervention or simulation. The ballerinas were reassessed using algometry and the Visual Analogue Scale (VAS) one week after the manipulation.

NCT ID: NCT04509869 Completed - Pain Clinical Trials

"Outcome of Varicocelectomy on Normal Semen in Patients Complaining of Orchialgia

Start date: August 12, 2017
Phase: N/A
Study type: Interventional

varicoclelectomy is done for subfertiltiy and varicocele induced orchialgia. The effect of varicocelectomy on semen analysis is controversial. Many articles report favorable outcomes and others do not. Most study don't focus on varicocelectomy done for varicocele induced orchialgia,and those studies dont report on postoperative semen. This study will focus on the effect of operation on the semen postoperatively .