Skip to content

Measurement of Crostin serum level after administration of Crocina tablet using HPLC technique

Measurement of Crostin serum level after administration of Crocina tablet using HPLC technique

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130507013263N2
Enrollment
5
Registered
2022-08-19
Start date
2022-06-05
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Evaluation of the concentration-time curve of the a Crostin in healthy people.

Interventions

Administration of one crocin tablet made by Samisaz company containing 15 mg of crocin orally..

Sponsors

Mashhad University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patient willingness to participate in the study Age above 18 years No addiction to narcotics, sedatives and alcohol No history of mental illness, no use of anticoagulants Absence of diabetes Absence of underlying disease

Exclusion criteria

Exclusion criteria: Hemodynamic instability in participant history of Cardiopulmonary resuscitation in participant past medical history of admission in the intensive care unit abnormal liver tests ( AST? ALT? CBC ) abnormal kidney tests ( U/A? BUN? Cr )

Design outcomes

Primary

MeasureTime frame
Determination of crostin blood concentration. Timepoint: Blood sampling will be done at 0, 30, 60, 90, 120, 180 and 240 minutes after drug administration. Method of measurement: Determination of crostin blood concentration by HPLC (High-performance liquid chromatography) system.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzin Hadizadeh

Mashhad University of Medical Sciences

hadizadehf@mums.ac.ir+98 51 3180 1128

Outcome results

None listed

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