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Valsalva Maneuver and Control in Reducing Pain During Spinal Injection

NCT04215276 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2020-02-21

No results posted yet for this study

Summary

The study aimed to compare the effectiveness of Valsalva maneuver as non pharmacological approach and control in reducing pain during spinal injection.

Conditions

  • Brachytherapy

Interventions

OTHER

Valsalva maneuver

pressure during Valsalva maneuver was measure using sphygmomanometer

OTHER

Control

patient was not given any intervention

Sponsors & Collaborators

  • Indonesia University

    lead OTHER

Principal Investigators

  • Alfan M Nugroho, MD · Indonesia University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-21
Primary Completion
2019-04-26
Completion
2019-04-26

Countries

  • Indonesia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04215276 on ClinicalTrials.gov