Skip to content

hebral nasal spray of vijayashwagandha for operation

Clinical Evaluation of Vijayashwagandha Nasal Spray As A Potent Perioperative Sedative Agent - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105124
Enrollment
30
Registered
2026-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: Z008- Encounter for other general examination

Interventions

None listed

Sponsors

Parul Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients ready to give informed consent. Patients of age group between 18-60 years of either gender. Patients of ASA grade I & II Patients planned elective surgery under local Anesthesia.

Exclusion criteria

Exclusion criteria: The patients falling within ASA grade III & IV. Pregnant and lactating women Mentally Retarded Patients

Design outcomes

Primary

MeasureTime frame
successful and timely completion of minor surgical procedure by means of effective ayurvedic sedationTimepoint: from commencement of sedation during procedure in between 10min 25min 45min 65min and 90min intraoperatively

Secondary

MeasureTime frame
total alcoholic extract of bhanga leaves and ashwagandha roots required to achieve sedative effect in patients degree of sedation by RASS scale hemodynamic indices including systolic blood pressure diastolic blood pressure pulse rate respiration rate and anxiety scoringTimepoint: occurrence of any adverse events and duration of stay from commencement of sedation and during procedure in between 10 minutes 25 minutes 45 minutes 65 minutes and 90 minutes intraoperatively observation of sedative effect postoperatively

Countries

India

Contacts

Public ContactDr Shubham Dhanesh Mishra

Parul Institute of Ayurveda

parikshit.shirode260038@paruluniversity.ac.in9175882746

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026