At a glance
ClinicalIndex Comparison RecordN/ACompleted· 30 enrolled
Drug / intervention
Meditationbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Decreasing Sedative Requirements for Peripheral Vascular Interventions Using Preoperative Guided Meditation
In Brief
A clinical study evaluating Meditation for Peripheral Vascular Disease. Completed, enrolled 30 participants across 4 sites.
Detailed Summary
The primary purpose of this clinical trial is to test the feasibility of implementing a perioperative guided meditation program for patients undergoing peripheral vascular interventions that are performed under procedural sedation and analgesia.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPeripheral Vascular Disease
CountriesUnited States
CollaboratorsAgency for Healthcare Research and Quality (AHRQ)
Timeline
N/ACompletedFinished
202420252026
First PostedMay 2023
Enrollment StartJul 2023
Primary CompletionDec 2023
Study CompletionApr 2024
TodayJul 2026
First PostedMay 1, 2023
Enrollment StartJul 11, 2023
Primary CompletionDec 11, 2023
Study CompletionApr 1, 2024
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 3.2 years ago
Interventions
Meditationbehavioral
Guided meditation utilizing breath awareness, body scan and visualization techniques