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The Effect of Dilution and Prolonged Injection Time on Dexamethasone-induced Perineal Irritation

NCT04950049 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2021-07-06

No results posted yet for this study

Summary

The purpose of this study is to investigate the efficacy of dilution with glucose and prolonged injection time on dexamethasone 21-phosphate induced perineal irritation (include pian and pruritus).

Conditions

  • Adverse Effect

Interventions

DRUG

Dexamethasone

receive 2ml dexamethasone (5mg/ml)

OTHER

Diluted dexamethasone 5ml

receive 5ml dexamethasone (2mg/ml) diluted with 5% glucose

OTHER

Diluted dexamethasone 10ml

receive 10ml dexamethasone (1mg/ml) diluted with 5% glucose

OTHER

Diluted dexamethasone 20ml

receive 20ml dexamethasone (0.5mg/ml) diluted with 5% glucose

Sponsors & Collaborators

  • General Hospital of Ningxia Medical University

    lead OTHER

Principal Investigators

  • Yonghai Zhang · General Hospital of Ningxia Medical University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2021-07-15
Primary Completion
2021-08-31
Completion
2021-08-31

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Drugs

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 NCT04950049 on ClinicalTrials.gov