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Oxidized Regenerated Cellulose and Voice Quality After Total Thyroidectomy

Effect of Oxidized Regenerated Cellulose on Voice Quality After Total Thyroidectomy: A Prospective Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07681557
Enrollment
30
Registered
2026-07-02
Start date
2014-01-01
Completion date
2014-08-31
Last updated
2026-07-02

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

Conditions

Postoperative Voice Change, Thyroid Diseases

Keywords

Oxidized regenerated cellulose, Surgicel, Total thyroidectomy, Recurrent laryngeal nerve, Voice quality, Acoustic voice analysis, Hemostasis, Postoperative voice change

Brief summary

This randomized controlled trial evaluated whether placement of oxidized regenerated cellulose (ORC) over the recurrent laryngeal nerves during total thyroidectomy affects early postoperative voice quality. Patients undergoing bilateral total thyroidectomy for benign or malignant thyroid disease were assigned in a 1:1 ratio to bilateral placement of ORC within the thyroid bed or to conventional hemostasis without ORC. All participants underwent preoperative videolaryngostroboscopic examination and objective acoustic voice analysis. Acoustic assessment was repeated on postoperative day 21. The study evaluated changes in jitter, shimmer, normalized noise energy, harmonics-to-noise ratio, maximum phonation time, and the s/z ratio. Postoperative complications and adverse events potentially related to ORC were also recorded.

Detailed description

This was a prospective, single-center, randomized, two-arm, parallel-group controlled trial involving patients undergoing bilateral total thyroidectomy for benign or malignant thyroid disease. Before surgery, all participants underwent videolaryngostroboscopic examination to document normal vocal cord mobility and recurrent laryngeal nerve function. Objective acoustic voice analysis was also performed before surgery. All operations were performed by the same experienced endocrine surgeon through a standard Kocher collar incision. Both recurrent laryngeal nerves and the parathyroid glands were routinely identified and preserved. Conventional hemostasis was achieved using bipolar cautery while avoiding thermal injury to the recurrent laryngeal nerves. Immediately before completion of surgery, participants were randomized in a 1:1 ratio using a simple card-drawing method performed by an assistant. In the experimental group, a 1 × 2 cm piece of oxidized regenerated cellulose was placed bilaterally over the recurrent laryngeal nerves within the thyroid bed. In the control group, surgery was completed after conventional hemostasis without placement of oxidized regenerated cellulose. Objective acoustic voice analysis was repeated on postoperative day 21 using 15-second voice recordings analyzed with Dr. Speech Real Analysis software. The assessed acoustic outcomes included jitter, shimmer, normalized noise energy, harmonics-to-noise ratio, maximum phonation time, and the s/z ratio.

Interventions

DEVICEOxidized Regenerated Cellulose

A sterile, absorbable topical hemostatic material. A 1 × 2 cm piece was placed bilaterally over the recurrent laryngeal nerves within the thyroid bed after conventional hemostasis had been achieved.

Sponsors

Ankara University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Single-center, two-arm, parallel-group randomized controlled trial with 1:1 allocation.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients scheduled to undergo bilateral total thyroidectomy for benign or malignant thyroid disease. * Written informed consent for participation. * Normal preoperative vocal cord mobility and recurrent laryngeal nerve function documented by videolaryngostroboscopic examination.

Exclusion criteria

* Previous thyroid surgery. * Previous parathyroid surgery. * Previous vocal cord surgery. * Previous laryngeal surgery. * Preoperative vocal cord paralysis. * Preoperative vocal cord polyp. * Any other preoperative laryngeal pathology considered likely to interfere with acoustic voice analysis.

Design outcomes

Primary

MeasureTime frameDescription
Change From Baseline in Jitter Percentage at Postoperative Day 21Baseline to postoperative day 21Jitter was calculated from a 15-second voice recording using Dr. Speech Real Analysis software and reported as a percentage. Change was calculated as the postoperative value minus the preoperative value.
Change From Baseline in Shimmer Percentage at Postoperative Day 21Baseline to postoperative day 21Shimmer was calculated from a 15-second voice recording using Dr. Speech Real Analysis software and reported as a percentage. Change was calculated as the postoperative value minus the preoperative value.
Change From Baseline in Normalized Noise Energy at Postoperative Day 21Baseline to postoperative day 21Normalized noise energy was measured using Dr. Speech Real Analysis software and reported in decibels. Change was calculated as the postoperative value minus the preoperative value.
Change From Baseline in Harmonics-to-Noise Ratio at Postoperative Day 21Baseline to postoperative day 21The harmonics-to-noise ratio was measured using Dr. Speech Real Analysis software and reported in decibels. Change was calculated as the postoperative value minus the preoperative value.
Change From Baseline in Maximum Phonation Time at Postoperative Day 21Baseline to postoperative day 21Maximum phonation time was measured in seconds during acoustic voice assessment. Change was calculated as the postoperative value minus the preoperative value.
Change From Baseline in the s/z Ratio at Postoperative Day 21Baseline to postoperative day 21The s/z ratio was calculated by dividing the maximum duration of sustained /s/ phonation by the maximum duration of sustained /z/ phonation. Change was calculated as the postoperative value minus the preoperative value.

Secondary

MeasureTime frameDescription
Number of Participants With Postoperative Surgical ComplicationsFrom surgery through postoperative day 21Postoperative complications included vocal cord paralysis, postoperative bleeding, wound infection, wound dehiscence, seroma, hypocalcemia, hypoparathyroidism, and local adverse reactions considered potentially related to oxidized regenerated cellulose.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 3, 2026