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Comparison of Benzydamine HCl 0.15% mouthwash and Ibuprofen effect on pain relief after crown lengthening, a clinical trial

Comparison of Benzydamine HCl 0.15% mouthwash and Ibuprofen effect on pain relief after crown lengthening, a clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016012312847N2
Enrollment
36
Registered
2016-03-02
Start date
2016-02-04
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

crown lengthing surgery.

Interventions

Intervention 1: Intervention group: rinse with benzydamine hydrochloride mouthwash 0.15% (the pharmaceutical company "Exir" Boroujerd) at a rate of once every 3 hours 15 ml for 30 seconds in mouth. In
Treatment - Drugs
Intervention group: rinse with benzydamine hydrochloride mouthwash 0.15% (the pharmaceutical company "Exir" Boroujerd) at a rate of once every 3 hours 15 ml for 30 seconds in mouth.
Control group: consume ibuprofen 400 mg tablets every 6 hours (the pharmaceutical company "Hakim").

Sponsors

Vice Chancellor for research of Shahid Sadooghi University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Periodontal health establishment? require crown lengthening surgery in the posterior teeth? avoiding the use of any painkiller or anti-inflammatory or Counter during the last 6 months? lack of systemic problems? lack of contraindications of ibuprofen or Benzydamine hydrochloride mouthwash. Benzydamine hydrochloride contraindications include hypersensitivity to the drug or formulation components? children under 12 years of age? past medical history and feed intake. Warning of eye contact with the drug. The classification used in pregnancy? is in category C. It should not be administered to a patient more than 7 days? and in case of allergies? medication should be discontinued. Information on medication safety in nursing mothers. Contraindications Ibuprofen include third trimester of pregnancy (the drugs X)? such as anaphylaxis or Angioedema history of severe allergic reaction caused by aspirin or other non steroidal anti-inflammatory drugs or nose polyp with spasticity due to an inflammatory disease or ulcerative the upper or lower gastrointestinal tract ? hemophilia and other blood disorders? including disorders of hemostasis? or platelets? kidney disorders ? stomatitis and elderly patients and patients the risk of gastrointestinal bleeding and ulcers in them is high. Concomitant use of ibuprofen with inhibitors of angiotensin converting enzyme (ACE)? one of the quinolone antibacterial agents? hypoglycemic sulfonylurea drugs? cyclosporine? lithium and methotrexate may? anticoagulants or thrombolytic? triamterene? valproic acid? aspirin and performance they interference is increasing or decreasing. Exclusion criteria: Unwillingness to participate in the plan? effective pain medications (analgesics or anti-inflammatory drug or drug) during the last 6 months? the risk of systemic problems affecting the periodontal tissues (diabetes? hypertension and heart disease? vascular)? ibuprofen is contraindicated or mouthwash Benzydamine hydrochloride.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 24 hours after intervention. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
Stingling & numbness. Timepoint: 24 hours after intervention. Method of measurement: asking from patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArezoo Khbazian

Shahid Sadooghi University Of Medical Sciences

arezookhabazian@yahoo.com; roseinthepalace@ymail.com+98 35 3625 0395

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 19, 2026