Evaluation the effect of Cichorium intybus L. on change the liver enzymes in burn patients

Evaluation the effect of Cichorium intybus L. on change the liver enzymes in burn patients: a randomized double- blind placebo-controlled clinical trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180609040016N1

Enrollment

Registered

2018-06-18

Start date

2018-07-23

Completion date

Unknown

Last updated

2018-07-16

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

Conditions

Liver disorder. Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: Intervention group: : Cichorium intybus L is bought from market of medicinal plants. Once verified by the botanist, it is used to prepare herbal extracts.so the Cichorium intybus L is

Eligibility

Sex/Gender

All

Age

20 Years to 75 Years

Inclusion criteria

Inclusion criteria: The burn time for patients is less than two days Their burn are is between 10% - 50% body surface percentage

Exclusion criteria

Exclusion criteria: The patients are not intubated No history for liver disease, hyperlipidemia, seizure No pregnancy

Design outcomes

Primary

Measure	Time frame
ALT level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;AST level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;?Albumin level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;CRP level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;Creatinin level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;Urea level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.	—

Measure

Time frame

ALT level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;AST level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;?Albumin level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;CRP level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;Creatinin level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.;Urea level. Timepoint: Every 3 days until discharg. Method of measurement: Biochemistry analysis.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbdlokhalegh Keshavarzi

Shiraz University of Medical Sciences

keshavarzi@sums.ac.ir+98 71 3230 5410

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026