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Impact of bilateral sphenopalantine ganglion block on intraoperative haemodynamic parameters in patients undergoing endoscopic pituitary surgery: A prospective randomized double blind study

Impact of bilateral sphenopalantine ganglion block with 0.5 percent ropivacaine versus saline on intraoperative haemodynamics in endoscopic pituitary surgery A prospective randomized double blind study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103904
Enrollment
60
Registered
2026-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Bilateral sphenopalantine ganglion block with 0.5% ropivacaine versus saline on intraoperative haemodynamics in endoscopic pituitary surgery.: 60 consenting patients fulfilling inclusio

Sponsors

Mahatma gandhi medical College and hospital sitapura jaipur rajasthan india
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient posted for elective endoscopic transnasal pituitary surgery needing general anaesthesia Patient of all genders patient aged between 18-65 years patient with american society of ASA CLASS I AND II

Exclusion criteria

Exclusion criteria: Patient with known or newly diagnosed coagulopathy patient with history of drug allergy to ropivacaine More than one attempt at SPG block contraindication to SPG block

Design outcomes

Primary

MeasureTime frame
To compare intraoperative haemodynamics parameters(heart rate and mean arterial pressure ) between patients receiving bilateral SPG block and those receiving placeboTimepoint: The effects will be assessed pre induction post induction post SPG block at 15 min intervals till 90 min and at the end of surgery

Secondary

MeasureTime frame
To assess the requirement of intraoperative rescue antihypertensive agents. To evaluate the need for additional anaesthetic agents (e.g.- propofol boluses) To assess the quality of surgical field as rated by the surgeon (using a standardized scale. e.g- Boezaart bleeding scale. To evaluate any adverse effects associated with SPG blockTimepoint: The effects will be assessed pre induction post induction post SPG block at 15 min intervals till 90 min & at the end of surgery

Countries

India

Contacts

Public ContactDr Shubham khandelwal

Dr. Shubham khandelwal

Shubham.kh29@gmail.com9799052551

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026