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Assessment of the effect of Levothyroxine on volume reduction of Benign thyroid nodule

Assessment of the effect of Levothyroxine in comparison to placebo on nodule Volume reduction in patients with benign thyroid nodule during six months follow up

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014030416828N1
Enrollment
60
Registered
2014-04-24
Start date
2014-04-04
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

Thyroid nodule. Disorders of thyroid gland

Interventions

Intervention 1: Intervention group:using Levothyroxine with Therapeutic dose of - 1/8 µgr/kg - daily- for six months. Intervention 2: Control group : half to one tablet daily for 6 months.
Treatment - Drugs
Placebo
Intervention group:using Levothyroxine with Therapeutic dose of - 1/8 µgr/kg - daily- for six months
Control group : half to one tablet daily for 6 months

Sponsors

Guilan University of Medical Sciences Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with single nodule or multi nodules ; that has been proved to be benign with FNA. Exclusion criteria: age under 20 and over 60 ; history of hypo and hyperthyroidism ; history of using Levothyroxine or other related drugs to thyroid ; pregnancy ; other diseases ( cardiovascular or liver disease )

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
TSH. Timepoint: before intervention and 6 weeks later and 6 months later. Method of measurement: laboratory kit.

Primary

MeasureTime frame
Thyroid nodule size. Timepoint: begining of assessment - six months later. Method of measurement: Ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSa'eed kalantari

Razi hospital

Dr_skalantari@gums.ac.ir+98 13 1554 1001

Outcome results

None listed

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