The effect of the propolis in oral wound healing

Clinical trial of comparison the effect of the propolis extract in combination with dressing without eugenol (Coe-Packtm) and Coe Packtm dressing in wound healing among patients undergoing crown lengthening surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016102630475N2

Enrollment

Registered

2017-02-09

Start date

2014-04-04

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

None listed

Interventions

Intervention 1: Control group: The patients washed their mouth before surgery with chlorhexidine 0.12% for 30 seconds. Lidocaine 2% with epinephrine 1:100000 (Septodont, France) were prescribed for lo

Treatment - Drugs

Control group: The patients washed their mouth before surgery with chlorhexidine 0.12% for 30 seconds. Lidocaine 2% with epinephrine 1:100000 (Septodont, France) were prescribed for local anesthesia,

Intervention group: The patients washed their mouth before surgery with chlorhexidine 0.12% for 30 seconds. Lidocaine 2% with epinephrine 1:100000 (Septodont, France) were prescribed for local anesthe

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: bone removal scale in their surgery was between 1-2 mm; their surgical time duration lasted between 90-115 minutes and had been used from both of chisels and bur in their surgery; don’t have any systematically problem; no periodontal disease in the surgical site; no restriction on surgery; don’t need to the antibiotic prophylaxis during the surgery; don’t use the corticosteroids or hormone in the last 2 months. Exclusion criteria: when there is a problem in recording the patient’s information; smoking.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 0,1,2,3,4,5,6 and 7 days after surgery. Method of measurement: Visual Analog Scale.;Burning sensation. Timepoint: 0, 1,2,3,4,5,6 and 7 days after surgery. Method of measurement: Visual Analog Scale.;Consistency of gingiva. Timepoint: 7th day after surgery. Method of measurement: palpation with a blunt instrument.;Colour compatibility. Timepoint: 7th day after surgery. Method of measurement: Visual Analog Scale.;Infection. Timepoint: 2nd & 7th days after surgery. Method of measurement: Clinical examination.;Bleeding during probing. Timepoint: 7th day after surgery. Method of measurement: Probing.	—

Measure

Time frame

Pain. Timepoint: 0,1,2,3,4,5,6 and 7 days after surgery. Method of measurement: Visual Analog Scale.;Burning sensation. Timepoint: 0, 1,2,3,4,5,6 and 7 days after surgery. Method of measurement: Visual Analog Scale.;Consistency of gingiva. Timepoint: 7th day after surgery. Method of measurement: palpation with a blunt instrument.;Colour compatibility. Timepoint: 7th day after surgery. Method of measurement: Visual Analog Scale.;Infection. Timepoint: 2nd & 7th days after surgery. Method of measurement: Clinical examination.;Bleeding during probing. Timepoint: 7th day after surgery. Method of measurement: Probing.

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Secondary

Measure	Time frame
-. Timepoint: -. Method of measurement: -.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtena Beiky

Dentistry faculty, Tehran University Of Medical Sciences

Atena. beiki69@gmail.com+98 21 5585 1131

Outcome results