Skip to content

Evaluation of the effectiveness of two methods: direct observation and avoiding nerve viewing in identifying the recurrent laryngeal nerve during thyroidectomy.

Evaluation of the effectiveness of two methods: direct observation and avoiding nerve viewing in identifying the recurrent laryngeal nerve during thyroidectomy.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251208068252N1
Enrollment
300
Registered
2026-02-26
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Damage to the recurrent laryngeal nerve. Paralysis of vocal cords and larynx, bilateral

Interventions

Intervention 1: Intervention group: On one side of the patient's neck during thyroidectomy, the recurrent laryngeal nerve (RLN) is systematically and completely exposed. Using standard thyroid surgery

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over 18 years of age who undergo thyroidectomy (partial or total) due to benign or malignant thyroid diseases. Patients who are able to undergo pre- and postoperative laryngoscopy. Informed consent of the patient to participate in the study and acceptance of the surgical procedure according to the study group (visual identification or IONM). Possibility of following patients for at least 30 days after surgery to assess nerve damage.

Exclusion criteria

Exclusion criteria: Patients with previous recurrent laryngeal nerve damage or chronic voice disorders. Patients who require concurrent surgery of the neck or adjacent areas, which can complicate the diagnosis of recurrent laryngeal nerve (RLN) injury. Patients who are unable to undergo postoperative laryngoscopy for any reason. Patients with neurological or muscular diseases that affect vocal cord function (such as myasthenia gravis or cranial nerve palsy). Patients who did not sign the study consent form or who withdrew from long-term follow-up.

Design outcomes

Primary

MeasureTime frame
Occurrence of recurrent laryngeal nerve palsy. Timepoint: Immediately after surgery (in the operating room) and 30 days after surgery (to determine whether it is temporary or permanent). Method of measurement: Evaluation of vocal cord function using direct laryngoscopy by the surgeon.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaman Afrasiabi

Qazvin University of Medical Sciences

samanafra@yahoo.com+98 28 3379 0643

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026