Randomize Clinical trial Comparison of the effect of Ibuprofen and Anaheal on pain control after periodental surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT201608301760N46

Enrollment

Registered

2016-09-21

Start date

2016-08-02

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

Pain after periodontal surgery. Other periodontal diseases

Interventions

Intervention 1: Intervention Groups: This group receive Anahel medicine after surgery one quaderant of the upper jaw. An hour before the surgery and six hours after one dose. Intensity of the pain

Treatment - Drugs

Intervention Groups: This group receive Anahel medicine after surgery one quaderant of the upper jaw. An hour before the surgery and six hours after one dose. Intensity of the pain will be assesse

Control Groups: This group receive Ibuprofen medicine after surgery another quaderant of the upper jaw. An hour before the surgery and six hours after one dose. Intensity of the pain will be asse

Eligibility

Sex/Gender

All

Age

No minimum to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who need Mucoperiosteal flap without bone surgery or with very limited surgery of two half maxillary bones Exclusion criteria: During the surgery outside for 45 minutes to 60 minutes; Patients with an allergy to any drugs or other NSA-IDs Ibuprofen and Anaheal; Asthma; A history of heart disease; Pregnancy; Patients with hemophilia; Gastrointestinal diseases such as peptic ulcer diseases; Kidney disease or liver; Coagulation disorders; Patients with systemic lupus erythematosus; Patients with any history of periodontal surgery in the last six months; Patients with severe fear and anxiety when visiting the dentist; Any analgesic use during the last 48 hours; Patients with age above 60 years; Alcohol and drugs; Total Rating Modified dental anxiety scale higher than nineteen

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: At 2, 4, 6, 8, 10, 12, 24 and 48 hours after surgery. Method of measurement: Visual Analogue scale(VAS) and Verbal Rating Scale(VRS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Reza Kazemi

Dental colleges of Tabriz

Rezakazemi_Dent88@yahoo.com+98 41 3335 7310

Outcome results

None listed

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