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Comparison of effectiveness between autologous Platelet-rich plasma and autologous fat with Platelet-rich fibrin in injection laryngoplasty for patients with unilateral vocal fold paralysis

Comparison of effectiveness between autologous Platelet-rich plasma and autologous fat with Platelet-rich fibrin in injection laryngoplasty for patients with unilateral vocal fold paralysis

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230227001
Enrollment
30
Registered
2023-02-27
Start date
2023-02-16
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients with unilateral vocal fold paralysis unilateral vocal fold paralysis, injection laryngoplasty ,Platelet-rich plasma, Fat, Platelet-rich fibrin

Interventions

The Platelet-rich plasma (PRP) was made by taking 10-20 ml of peripheral blood from patient. Blood is then inserted to tube and centrifuge with 1500 rpm for 10 min then the PRP was extracted under ste
s abdomen to create the filler ( Fat with PRF ) for injection laryngoplasty under general anesthesia in operating room
Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery
autologous Platelet-rich plasma,autologous fat with Platelet-rich fibrin

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Unilateral vocal fold paralysis patients with 6 months onset is considered to injection laryngoplasty for treatment 2.Willing to give consent

Exclusion criteria

Exclusion criteria: 1.Age < 18 years 2.Patients with bleeding tendency or coagulopathy. 3.Patient isn't able to follow up as research protocol. 4.Patients received phonosurgery before. 5.Organic lesions were found, e.g., vocal polyps, vocal tumor, vocal cyst,or glottic cancer. 6.Patients with cricoarytenoid joint fixation or fibrosis at posterior vocal cord. 7.Patients who don't have enough fat for harvestment. 8.Patients who refuse to enroll the study

Design outcomes

Primary

MeasureTime frame
Voice handicap index (VHI) preoperative, postoperative at 1 month and 6 month Questionnaire of VHI score

Secondary

MeasureTime frame
Jitter preoperative, postoperative at 1 month and 6 month Dr.speech equipment,Shimmer preoperative, postoperative at 1 month and 6 month Dr.speech equipment,NHR preoperative, postoperative at 1 month and 6 month Dr.speech equipment,MPT preoperative, postoperative at 1 month and 6 month Dr.speech equipment

Countries

Thailand

Contacts

Public ContactVanusanan Sudsamai

Faculty of Medicine Ramathibodi Hospital, Mahidol University

Bo.vanusanan@gmail.com0948986249

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026