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Randomised parallel study against placebo for the determination of efficacy of liophilised Salvia Officinalis and Helichrysum italicum in pain treatment from post-surgery pain in 45 male or female patients.

Randomised parallel study against placebo for the determination of efficacy of liophilised Salvia Officinalis and Helichrysum italicum in pain treatment from post-surgery pain in 45 male or female patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2005-000958-71-IT
Enrollment
Unknown
Registered
2005-06-07
Start date
2005-03-24
Completion date
Unknown
Last updated
2012-03-19

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

Conditions

Pain treatment. MedDRA version: 6.1 Level: PT Classification code 10048459

Interventions

Product Name: freeze-dried extract of sage leaf (Salvia officinalis) Product Code: ABO/SAL Pharmaceutical Form: Granules for oral suspension CAS Number: NA Current Sponsor code: ABO/SAL Other descript

Sponsors

ABOCA
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Main Objective: ;Secondary Objective: ;Primary end point(s):—

Countries

Italy

Outcome results

None listed

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