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Seated Time for 90% Incidence of Hypotension

R

Royal Victoria Hospital, Canada

Status

Unknown

Conditions

Cesarean Section Complications

Treatments

Other: seated time

Study type

Interventional

Funder types

Other

Identifiers

NCT03113045
15010MUHC

Details and patient eligibility

About

The study will determine the 90% effective seated time after intrathecal injection of hyperbaric bupivacaine to avoid hypotension in patients undergoing cesarean delivery.

Full description

The study will use a Biased Coin Design (BCD), up-and-down sequential method, to determine the ET90 for absence of hypotension during Cesarean delivery. In this methodology, the first patient will be assigned an a priori initial seated time. Any other patient will be assigned a seated time based on the presence or absence of hypotension in the previous patient. If the previous patient developed hypotension, then the new patient will be seated for a longer time, which will be equal to the seated time of the previous patient plus a pre-determined time increment (up to an also pre-determined maximum allowed time). If no hypotension occurred to the previous patient, the new patient will be assigned one seated time from two choices: The same seated time that has been assigned to the previous patient, or a seated time shorter than that of the previous patient by a pre-determined time decrement (the pre-determined time increment and decrement are the same). The choice will be determined from a biased coin result, with a probability of 0.9 for assigning 'the same as previous' seated time and a probability of 0.1 for assigning a 'shorter seated time'.

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with singleton pregnancies scheduled for elective cesarean delivery

Exclusion criteria

  • BMI>35
  • Unable to communicate in study language
  • ASA greater than 2
  • Hypertensive disease of pregnancy

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Seated Time
Experimental group
Description:
Pts will be seated for the allocated time depending on the previous patients hypotensive response
Treatment:
Other: seated time

Trial contacts and locations

1

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Central trial contact

Albert Moore

Data sourced from clinicaltrials.gov

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