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Procedural Anxiety clinical trials

View clinical trials related to Procedural Anxiety.

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NCT ID: NCT05895383 Recruiting - Procedural Pain Clinical Trials

Self-Adjusted Nitrous Oxide: A Feasibility Study in the Setting of Vasectomy

SANO-VAS
Start date: May 24, 2023
Phase: Phase 4
Study type: Interventional

This study is being done to see if nitrous oxide during vasectomy decreases pain and anxiety, and also assess whether patients have better satisfaction when they control their own level of nitrous oxide during the procedure. If we find that patients experience less pain or anxiety with nitrous oxide, it could be suggested that self-adjusted nitrous oxide (SANO) may be a useful tool for improving experience of care during vasectomy.

NCT ID: NCT05267704 Recruiting - Pain, Procedural Clinical Trials

Evaluating the Feasibility of VR for Pediatric Renal Biopsies

Start date: October 11, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the use of virtual reality (VR) as an adjunct or alternative to pharmacologic sedation in pediatric patients undergoing renal biopsy.

NCT ID: NCT04571879 Recruiting - Procedural Pain Clinical Trials

Nebulized Lidocaine and Intranasal Midazolam for NGT Insertion in Children

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

Nasogastric tube (NGT) is a commonly performed procedure in the Emergency Department. Although it is not a major procedure, it is usually associated with a bad experience and cause discomfort and pain in kids. This randomized controlled double-blinded double-dummy trial aims to investigate the efficacy of local topical anesthetic and/or anxiolysis for pain/anxiety related to NGT insertion. Eligible patients are children with gastroenteritis aged 6 months to 5 years requiring NGT rehydration. The intervention are 3 arms of nebulized lidocaine with midazolam compared to nebulized midazolam alone or placebo. The primary outcome is procedure-related pain assessment using the Face, Legs, Activity, Cry, and Consolability (FLACC) scale during final NGT insertion attempt.

NCT ID: NCT04471402 Recruiting - Dexmedetomidine Clinical Trials

Determining the Pharmacogenetic Basis of Non-responsiveness to the Sedative Effects of Dexmedetomidine in Children

Start date: July 20, 2020
Phase:
Study type: Observational

Intranasal Dexmedetomidine is one of the sedative drugs of choice commonly used as an anxiolytic premedication for children for diagnostic or therapeutic procedures. However, some children do not achieve the level of sedation expected with the usual dose after an expected timeframe, leading to distress and costly time wasted. In this study, we would try to identify a genetic basis to non-responders of Dexmedetomidine by comparing a chosen gene panel of 250 relevant genes between responders and non-responders to a standardized 3mcg/kg intranasal Dexmedetomidine.

NCT ID: NCT04203082 Recruiting - High Risk Pregnancy Clinical Trials

Cognitive Behavioral Intervention to Reduce Procedural Anxiety Among Woman With High Risk Pregnancies With Scheduled Cesarean Deliveries

Start date: July 23, 2020
Phase: N/A
Study type: Interventional

The goals of this study are to determine the feasibility and efficacy of a brief, single-session cognitive-behavioral intervention for reducing preoperative and postoperative anxiety and for determining satisfaction with the delivery process in pregnant women scheduled for Cesarean delivery due to complications with their pregnancy. This will be done through a combination of psychoeducation and exposure therapy, where the participants will be walked through the steps of a Cesarean delivery in an operating room that mimics where the patient would actually be delivering. Follow-up will occur during the immediate and extended postpartum periods to determine satisfaction and levels of anxiety.

NCT ID: NCT03740607 Recruiting - Procedural Pain Clinical Trials

Virtual Reality for Alleviation of Peripheral IV Placement-Associated Discomfort

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

Immersive virtual reality (iVR) has been used successfully to manage pain with distraction. It is a non-invasive treatment modality unassociated with worrisome well-known side effects typically seen when opioids and NSAIDS are used, and has previously been used safely in place of analgesia during dressing changes and burn care. This study investigates whether iVR can be useful as a stand-alone option to manage the pain associated with placement of peripheral intravenous (PIV) catheters in adults.