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Clinical study of the analgesic effect of borneol in patients with postoperative pain

Clinical study of the analgesic effect of borneol in patients with postoperative pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009714
Enrollment
Unknown
Registered
2016-11-02
Start date
2015-06-02
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

postoperative pain

Interventions

Borneol group:topical application
Placebo group:topical application

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 85 years at the day 2 or day 3 after surgery and had a postoperative pain with a score of at least 3 on a 10 visual analog scale (VAS).

Exclusion criteria

Exclusion criteria: (1) Patient who refuses to participate the study; (2) Patient with wound infection; (3) Patient who is psychopath or without clear consciousness; (4) Patient who allergic to ethanol or borneol; (5) Patient who is participating other clinical studies; (6) Patient who is considered not appropriate for inclusion.

Design outcomes

Primary

MeasureTime frame
VAS score of pain intensity;—

Countries

China

Contacts

Public ContactDan Zhang

Shanghai Changzheng Hospital

zhangadanbama@hotmail.com+86 18616184746

Outcome results

None listed

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