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Blood pressure control in both intravenous and inhalation anesthetics in sinus surgery

Comparison of blood pressure control in two general anesthetics technique of isoflurane and propofol in two anti hypertensive nitroglycerine-Labetalol or remifentanil in functional sinus endoscopic surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017102715108N3
Enrollment
84
Registered
2017-11-19
Start date
2017-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Blood pressure. Elevated blood-pressure reading, without diagnosis of hypertension

Interventions

Intervention 1: Intervention group 1: Patients undergoing inhaled anesthetic of isoflurane and receive nitroglycerine-Labetalol. Intervention 2: Intervention group 2: Patients undergoing inhaled anest
Treatment - Drugs
Intervention group 1: Patients undergoing inhaled anesthetic of isoflurane and receive nitroglycerine-Labetalol.
Intervention group 2: Patients undergoing inhaled anesthetic of isoflurane and receive remifentanil.
Intervention group 3: Patients undergoing vein anesthetic of propofol and receive nitroglycerine-Labetalol.
Intervention group 4: Patients undergoing vein anesthetic of propofol and receive remifentanil.

Sponsors

Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients undergoing functional sinus endoscopic surgery that should have a systolic blood pressure of more than 100 and an arterial hypertension above 55. Exclusion criteria: Patients with history of hypertension; antihypertensive drugs; addicted patients; use of neurological drugs; patients with coagulation disorder and anticoagulants.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Amount of blood pressure. Timepoint: At the entrance to the operating room, after the induction, 15, 30, 45, 60, 75, 90, and 105 minutes during surgery. Method of measurement: In mmHg using a mercury barometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Reza Safaeian

Iran University of Medical Sciences

rezasafa@yahoo.com+98 21 4464 0531

Outcome results

None listed

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