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Evaluation of thyroid Surgery Outcomes with and without drain

Clinical trials comparison of complications of thyroid surgery with and without drain

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016030319255N4
Enrollment
180
Registered
2016-06-08
Start date
2013-01-01
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 diseases caused by iodine deficiency. Iodine deficiency related thyroid disorders

Interventions

Intervention 1: In intervation group, the patients that are condidated for total or subtotal or lobectomy of thyroid surgery is drained.The hemovac drain is passed from below the neck incision. Based
decide to bring out in the days after the operation. Intervention 2: In the control group after thyroid surgery is not drained. Patients are examined days after surgery and are discharged on the basis
Treatment - Surgery
In intervation group, the patients that are condidated for total or subtotal or lobectomy of thyroid surgery is drained.The hemovac drain is passed from below the neck incision. Based on the patient's
decide to bring out in the days after the operation.
In the control group after thyroid surgery is not drained. Patients are examined days after surgery and are discharged on the basis of general conditions.

Sponsors

Vice Chancellor for Research and Technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with a diagnosis of thyroid cancer; Multinodular goiter and thyroid nodules; undergoing total or subtotal or lobectomy of thyroid surgery . Inclusion criteria: patients with a diagnosis of thyroid cancer; Multinodular goiter and thyroid nodules; undergoing total or subtotal or lobectomy of thyroid surgery . pleased to participate in the study; Exclusion criteria were: if patients in the preoperative studies, have an underlying disease (diabetes, cardiovascular disease, etc.); congenital; acquired bleeding disorder; retrosternal thyroid; patients who underwent modified or radical neck dissection or forced to devise the drains were during surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hematoma surgery. Timepoint: Hospitalization time and first postoperative visit. Method of measurement: Evaluation by surgen or surgical resident.;Infection surgery. Timepoint: Hospitalization time and first postoperative visit. Method of measurement: Evaluation by surgen or surgical resident.

Secondary

MeasureTime frame
Need surgery to drain the hematoma. Timepoint: Hospitalization time and first postoperative visit. Method of measurement: Clinical diagnosis of assistant surgeon or surgical resident.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Asgari Abbaszadeh

Babol University of Medical Sciences

Asgari2429@gmail.com+98 11 3225 6285

Outcome results

None listed

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