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Effect of Curcumin in Adenotonsillectomy pain reduction

Study of the efficacy of Turmeric oil oral spray (Curcumin) on reduction of post Adenotonsillectomy pain in 4-12 years old children: three blind randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130713013976N6
Enrollment
122
Registered
2018-12-05
Start date
2018-10-23
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Adenotonsillar hypertrophy.

Interventions

Intervention 1: Intervention group: The surgical site is rinsed, then use aTurmeric spray spray at 2 puffs one minute before surgery and use the same amount of spray immediately after surgery, then us

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 12 Years

Inclusion criteria

Inclusion criteria: Patients undergoing Adenotonsillectomy Age 4 to 12 years of both sexes

Exclusion criteria

Exclusion criteria: Sensitivity to Turmeric Using cautery during surgery In the absence of understanding the pain assessment images by the child and the inability to intervene and lack of parental support Any known systemic disease, such as congenital anomalies, bleeding disorders, type 1 diabetes, kidney disease, colds, and fever

Design outcomes

Primary

MeasureTime frame
Scale of sore throat in the Visual Analog Scale (VAS). Timepoint: Measurement of sore throat in the first 5 days after Adenotonsillectomy. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
The frequency of use of prescribed acetaminophen intake. Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.;Having or not having ear pain (autoelastic). Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.;Tolerate normal diet. Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.;Having or not having nausea. Timepoint: In the first 5 days after Adenotonsillectomy. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasser Bahari

Hamedan University of Medical Sciences

naser.bahaari.medicalstudent@gmail.com+98 939 822 5654

Outcome results

None listed

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