FindTrial
Sign In

Prophylactic efficacy of intravenous atropine with crystalloid co-loading to prevent post-spinal hypotension in parturient undergoing cesarean delivery at Dilla University Referral Hospital, Southern Ethiopia, 2017

Prophylactic efficacy of intravenous atropine with crystalloid co-loading to prevent post-spinal hypotension in parturient undergoing cesarean delivery at Dilla University Referral Hospital, Southern Ethiopia, 2017

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202002753328352
Enrollment
82
Registered
2020-02-21
Start date
2017-01-15
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Pregnancy and Childbirth

Interventions

Atropine group
Saline group

Sponsors

Dilla University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Term pregnancy ASA I & II pregnant mothers Age above 18.

Exclusion criteria

Exclusion criteria: Hypertensive disorders of pregnancy (eclampsia, pre-eclampsia) Known diabetic patient Mothers on beta blockers and any other drug which alter response of study drug Baseline heart rate 120 beat per minute Febrile patient Age greater than 40 years Spinal anesthesia converted to general anesthesia because of total spinal or inadequate block

Design outcomes

Primary

MeasureTime frame
Incidence of hypotension between groups—

Secondary

MeasureTime frame
Total crystalloid consumption between groups;Time to development of hypotension—

Countries

Ethiopia

Contacts

Public ContactFistum Solomon

Assistant profesor

fistumsbr@gmail.com+251911763711

Outcome results

None listed

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