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The effect of Damperli herbal drop on Sinusitis

Effects of Damprly herbal drops for the treatment of sinusitis patients with acute sinusitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016122131510N1
Enrollment
50
Registered
2017-01-16
Start date
2016-11-21
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

Acute sinusitis. Acute sinusitis

Interventions

Placebo
Intervention 1: Controls: placebo drops of distilled water or NaCl which will be used as a drop Damprly consumed.routine treatment of sinusitis, including antibiotic Co-amoxiclav (if the sensitivity o
Treatment - Drugs
Controls: placebo drops of distilled water or NaCl which will be used as a drop Damprly consumed.routine treatment of sinusitis, including antibiotic Co-amoxiclav (if the sensitivity of Cefixime), ser
Invention: drop Damprly be used. routine treatment of sinusitis, including antibiotic Co-amoxiclav (if the sensitivity of Cefixime), serum washing (2-3 times a day) and Fluticasone spray is carried o

Sponsors

iranian academic center for education, culture and research, ardabil branch
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 90 Years

Inclusion criteria

Inclusion criteria: Study inclusion criteria will be as follows: 1. the patient is not under 7 years. 2.there is no history of certain diseases. 3. The patient is not pregnant. 4. The patient is not breast feeding. Exclusion criteria were studies will be as follows: 1- self-satisfaction. 2-allergy Damperly herbal drops sensitive type.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Facial pain / pressure. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Facial congestion / fullness. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Nasal obstruction / blockage. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Nasal discharge / purulence, discolored posterior drainage. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Hyposmia / anosmia. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Purulence on nasal examination. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Fever (acute rhinosinusitis only). Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.

Secondary

MeasureTime frame
Headache. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Fever (nonacute rhinosinusitis). Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Halitosis. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Dental pain. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Cough. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.;Ear pain / pressure / fullness. Timepoint: Before and two weeks after the intervention. Method of measurement: Find out - Photos - CT.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahmud Khorushy

S. W. A. Co.

azhyaneh.co@gmail.com+98 45337495038

Outcome results

None listed

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