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Effect of anaheal in reducing complication of sinus lift

Comparison of the effectiveness of anaheal and iboprofen in reducing the complications of sinus lift surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181114041651N3
Enrollment
20
Registered
2024-11-20
Start date
2024-11-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

maxillary sinus lift surgery. Complete loss of teeth

Interventions

Intervention 1: Intervention group: In addition to ibuprofen 400mg, amoxicillin 500mg and metronidazole 250mg ( 3 times a day for one week), the study group should also receive Anahil 500mg capsules o

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: People willing to participate in the study and required to complete the informed consent form developed by the researcher Sinus lift surgery for implant placement is mandatory and unavoidable

Exclusion criteria

Exclusion criteria: Systemic diseases that prevent wound healing in the usual way, including diabetes and diseases that weaken the immune system, and the use of anticoagulants and bisphosphonates. certain habits that cause a change in the intensity of bleeding or wound healing, including smoking and alcohol. No exciting to participate in the study and refusing to complete the informed consent form. Allergy to pineapple and turmeric and a history of symptoms such as nausea and skin hives caused by allergy to this fruit pregnancy Mental and physical problems of the patient History of radiotherapy or candidate for radiotherapy local infection Periodontitis of destructive adjacent teeth Receiving an antibiotic regimen by a doctor during the last month

Design outcomes

Primary

MeasureTime frame
Swelling. Timepoint: The third and seventh day after surgery. Method of measurement: The amount of swelling reduction is calculated according to facial indices such as: the line connecting the sub_nasion and the tragus and the line connecting the sub_nasion to the outer canthus of the eye and its intensity is compared in the control group and the study group.;Pain. Timepoint: The third and seventh day after surgery. Method of measurement: The amount of pain caused by surgery is calculated using the VAS index. And its intensity is compared in the control group and the study group.;Bruise. Timepoint: The third and seventh day after surgery. Method of measurement: The amount of bruising on the face is divided into three categories: low (bruise smaller than 2 mm), medium (bruise between 2 and 4 mm) and high (bruise more than 4 mm). And its intensity is compared in the control group and the study group.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan Aliabadi

Shiraz University of Medical Sciences

aliabadie@sums.ac.ir+98 917 314 0896

Outcome results

None listed

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