ondasterone during spinal anathesia for elective caeserian section

the effect of ondasterone versus placebo in reduction of hypotension during spinal anathesia for elective cesarean section:a prospective rando mixes trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201601001397193

Enrollment

100

Registered

2015-12-21

Start date

2015-12-21

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Surgery Fertility-female

Interventions

ondasterone

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Elective cs

Exclusion criteria

Exclusion criteria: Hypersensitivity to ondasterone Contraindicated spinal anathesia

Design outcomes

Primary

Measure	Time frame
pulse.blood presume. oxygen saturation.nausea and vomiting	—

Secondary

Measure	Time frame
vasopressin dose nausea and vomiting	—

Countries

Egypt

Contacts

Public Contactnabih elkhouly

lecturer of obstetrics and gynecology department.Faculty of medicine.menoufia university

nabih.elkhouly@yahoo.com01060868443

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026