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Evaluating the efficacy of Bromelain on donor wound healing after free gingival surgery

Evaluating the efficacy of Bromelain on donor wound healing after free gingival surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201502089002N5
Enrollment
26
Registered
2015-03-15
Start date
2014-03-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Gingival recession. Gingival recession (generalized)(localized)(postinfective)(post-operative)

Interventions

Intervention 1: Intervention group : Bromelain (capsule 500mg, oral , once a day for 10 days ). Intervention 2: Control group : placebo (capsul , oral , once a day for 10 days ).
Treatment - Drugs
Intervention group : Bromelain (capsule 500mg, oral , once a day for 10 days )
Control group : placebo (capsul , oral , once a day for 10 days )

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: In this study , individuals who refer to treatment of gingival recession in the anterior site of the mandible that candidate to free gingival graft surgery and have thease criteria will choose: -One of the mandibullar central incisor has Miller class 1,2 or 3 gingival recession. -Systemically healthy -Don't use anticoagulatory drugs like Warfarin. - Didn't use antibiotic and corticosteroid at least during the past tow months. -Aren't smoker or don't smoke more than 10 cigarette. -The mesdames aren't pregnant or lactiferrous .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Complete epithelialization of donor site. Timepoint: 7 days after surgery ang 10 days after surgery. Method of measurement: To evaluate of epithelialization, 3% hydrogen peroxide apply to the wound by a brush. If the epithelialization is completed, then hydrogen peroxide dose not diffuse into the connective tissue, and oxygen is not librated, ther for any bubble dose not observe.Otherwise , the epithelialization isn't completed.;Pain. Timepoint: 7 days after surgery. Method of measurement: VAS.;The number of analgesic tablets that take by the patients. Timepoint: 7 days after surgery. Method of measurement: the number that reported by the patients.

Secondary

MeasureTime frame
Bleeding. Timepoint: 7 days after surgery. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahime khoshkhooie

School of dentistry

fahime_khoshkhooie68@yahoo.com+98 81 3838 0572

Outcome results

None listed

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