Skip to content

A Clinical trial to study the effect of two drugs on Postoperative pain, Bupivacaine and other Bupivacaine with Dexmedetomidine with Normal saline in Patient undergoing Functional Endoscopic Sinus Surgery

Efficacy of Bilateral Sphenopalatine ganglion block on Postoperative Pain in Patient undergoing Functional Endoscopic Sinus Surgery - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104495
Enrollment
90
Registered
2026-02-23
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: G891- Acute pain, not elsewhere classified

Interventions

Intervention1: Nil: Nil Intervention2: Bupivacaine with Dexmedetomidine is added to one of the group. Dexmedetomidine , an alpha 2 adrenergic agonist, is believed to work by inhibiting the release of

Sponsors

Dr Kairavi Ranipa
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 18 and 65 years either sex American society of Anaesthesiologist Physical status 1 or 2 Able to understand the study protocol and willing to provide written informed consent

Exclusion criteria

Exclusion criteria: Pregnent and Lactating women Body Mass Index more than 30 Patient taking regular analgesic or antidepressant or antiepileptic History of drug allergy Coagulopathy disorder Infection at site of injection Patient refusal Uncontrolled HTN or DM or Cardiovascular otr Cerebrovascular or Endocrine or Renal or Liver disease

Design outcomes

Primary

MeasureTime frame
Compare the efficacy of Bupivacaine alone,Bupivacaine + Dexmedetomidine and Normal saline in Sphenopalatine ganglion block in patient undergoing FESSTimepoint: After 2 hours,4 hours, 8 hours, 12 hours and 24 hours

Secondary

MeasureTime frame
NilTimepoint:

Countries

India

Contacts

Public ContactDr Vandana Parmar

Pdu civil hospital Rajkot

drvandanapithadia@yahoo.com9898090220

Outcome results

None listed

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