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Effects of bromelain and serrapeptase supplementation on surgical and traumatic wound healing and pain reduction

Effects of bromelain and serrapeptase supplementation on surgical and traumatic wound healing and pain reduction (a double blind randomized controlled trial)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140804018677N6
Enrollment
80
Registered
2021-02-15
Start date
2021-02-28
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

trauma. Acute pain due to trauma

Interventions

Intervention 1: Intervention group: Eating bromelain/serrapeptase capsules (250 mg bromelain and 30 mg serrapeptase per cap) BD (every 12 hours) for 10 days. Capsules are manufactured in "Dayan Teb Ek

Sponsors

Research and technology deputy, Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Male and non-pregnant female age>18y Up to 1 week post trauma or surgery Wound size between 1-10 cm tend to use this supplement

Exclusion criteria

Exclusion criteria: Allergy to bromelain and serrapeptase Collagen Vascular or autoimmune Diseases mild-moderate and severe wound according to American infectious disease society criteria Using steroidal drugs in 2 months prior to study (exp. inhaled steroidal drugs for COPD and asthma and topical steroidal medication Using antibiotics in a week prior to study radiation therapy of wound HBA1c>10 venous insuf?ciency or osteomyelitis Using immunosuppressant active malignancies Renal disorders ((blood urea nitrogen < 21.4 mmol/l, creatinine < 247.5 umol/l) or liver failure MI in 3 months prior to study Drug or alcohol abuse

Design outcomes

Primary

MeasureTime frame
Pain of wound (trauma or surgical). Timepoint: Baseline and at the end of the study. Method of measurement: VAS (visual analog scale).;Size of wound (trauma or surgical). Timepoint: Baseline and at the end of the study. Method of measurement: Centimeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoodeh Razeghi Jahromi

Shahid Beheshti University of Medical Sciences

soodehrazeghi@gmail.com+98 21 2235 7483

Outcome results

None listed

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