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Effect of sitting position on blood pressure reading among patients for caesarean section under spinal anesthesia

Maximum allowable sitting time following spinal anaesthesia for elective caesarean section and its effect on incidence of hypotension

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000472875
Enrollment
90
Registered
2012-04-30
Start date
2012-04-14
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

To assess the effect of sitting position following spinal anesthesia for elective caeserian section on hypotension, dermatomal level, and duration of spinal block. Four groups of patients will be studied. One will be allowed to set for 3 (control group), 5 min, second for 7 min, and the third for 9 min

Interventions

After approval of ethics committee of King Abdul Aziz university hospital, informed, written consent will be obtained from 90 ASA class I or II patients undergoing elective caesarean section. IV cannula will be established. 500 mL of 6% hydroxyethyl starch 130/0.4 (voluven) will be administered over 20 min. combined epidural- spinal anesthesia will be performed. 10 mg of heavy bupivacaine 0.5% mixed with 20 micro g fentanyl will be injected into the subarachnoid space without any injection via

After approval of ethics committee of King Abdul Aziz university hospital, informed, written consent will be obtained from 90 ASA class I or II patients undergoing elective caesarean section. IV cannula will be established. 500 mL of 6% hydroxyethyl starch 130/0.4 (voluven) will be administered over 20 min. combined epidural- spinal anesthesia will be performed. 10 mg of heavy bupivacaine 0.5% mixed with 20 micro g fentanyl will be injected into the subarachnoid space without any injection via epidural catheter. following that patients were randomly assigned into one of three equal groups of thirty patients each by using sealed envelope method. The randomization was dependent on the time allowed for each patient to be maintained on sitting position after intrathecal injection. In the four groups (group A, B, C and D) the patients were maintained in sitting position for 3, 5, 7 and 9 minutes consequatively before turning them into supine position. 3 min time was considered as a control group.

Sponsors

King Abdulaziz University Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

ASA class I or II patients undergoing elective caesarean section, obtained consent

Exclusion criteria

obesity, preexisting hypertension, pregnancy-induced hypertension, known cardiovascular or cerebrovascular disease, abnormal cardiotocography (CTG) tracing, or patients with contraindications to spinal anesthesia

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026