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Testing Bhanga (Cannabis) Powder Before Surgery in Mouth Cancer Patients Phase 1 Study

Phase 1 study of safety and feasibility of Bhanga (Cannabis sativa) churna in the Pre-operative period in oral cavity squamous cell cancer. - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106030
Enrollment
25
Registered
2026-03-12
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: C060- Malignant neoplasm of cheek mucosa

Interventions

None listed

Sponsors

AYUSH CoE, Ministry of Ayush, Government of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Histo-pathologically proven patients of oral cavity SCC. Only clearly operable cancers planned to undergo upfront curative surgery. Patient fit for surgery (ASA Grade I / II). Patient voluntarily willing to give consent for study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
1.The study will generate hypotheses for future investigation of Bhanga churna in the preoperative period to achieve improved clinical outcomes of OCSCCTimepoint: Baseline Day 21 Day 49

Secondary

MeasureTime frame
2. Pharmacokinetic modelling Timepoint: Day 1 Predose 30 min 1Hour 1.5 Hour 2 Hour 4 Hour 6 Hour Day 21 Predose 30 min 1Hour 1.5Hour 2 Hour 4 Hour 6 Hour Before Surgery At the end of surgery Post-operative Day 01 Post-operative Day 02 Post-operative Day 03 Post-operative Day 14 ;Transcriptomic AnalysisTimepoint: Day 1 (Before dose intake) Day 22 (On the day of surgery) Before Surgery During Surgery At the end of Surgery

Countries

India

Contacts

Public ContactDr Vikram Gota

Advanced Centre for Treatment, Research and Education in Cancer (ACTREC)

vikramgota@gmail.com02227405493

Outcome results

None listed

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