Evaluation of labor analgesia effect and intervention effect of adverse reaction: a randomized controlled trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900022688

Enrollment

Unknown

Registered

2019-04-22

Start date

2019-05-01

Completion date

Unknown

Last updated

2019-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

labor analgesia

Interventions

Experimental group:Intravenous giving to Dexamethasone 5mg

Experimental group 2:Intravenous giving to Dexamethasone 10mg

Control group:Intravenous giving to 0.9% Nacl Saline

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Meet the requirements of natural delivery, have the will to do painless delivery of the first maternity.

Exclusion criteria

Exclusion criteria: A history of digestive tract, central nervous system and other systemic diseases that may cause nausea and vomiting; the use of anti-vomiting drugs in the 48h before surgery; uncontrolled diabetic patients; and the contraindications of Intraspinal block.

Design outcomes

Primary

Measure	Time frame
nausea;vomiting;fever;blood glucose;	—

Countries

China

Contacts

Public ContactLiying Zhan

Department of Anesthesiology, Renmin Hospital of Wuhan University

xcensure@126.com+86 15327408448

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026