Efficacy and Safety of Prunella Oral Liquid in the Treatment of Thyroid Nodules

Official title

Efficacy and Safety of Prunella Oral Liquid in the Treatment of Thyroid Nodules: a Multicenter, Prospective, Randomized, Double-blind, Placebo-controlled Study

Overview

A multicenter, prospective, randomized, double-blind, placebo-controlled clinical trial was designed to evaluate the efficacy and safety of Prunella oral liquid in patients with benign thyroid nodules, which belongs to the post-marketing reevaluation clinical study. In this study, 234 subjects will be enrolled by competitive enrollment at several research centers across China. The main inclusion criteria are: ① Thyroid ultrasound examination found thyroid nodules, can be accompanied by goiter, and the nodules meet the following conditions: 1) There were dominant nodules in single or multiple nodules (the largest diameter of the second largest nodules was not more than 50% of the largest nodules), 2) solid nodules, 3) the longest diameter of nodules was ≥1cm and \< 3cm, 4) C-TIRADS 3\~4A nodules. ② Patients who met the puncture indication were confirmed by fine needle aspiration biopsy (FNAB) as benign nodules (Bethesda II). ③ Levels of TSH, FT3 and FT4 were normal, and the antibody titers of TgAb and TPOAb were normal. Eligible subjects will be randomly assigned on a 1:1:2:2 scale to: Group A (placebo conventional dose group, 10 mL/times, 2 times/day), group B (placebo 2x dose group, 10ml/times, 2 times/day), group C (conventional dose group of Prunella oral liquid), group D (Prunella oral liquid 2x dose group). All subjects will receive the treatment for 9 months and follow up at 3rd, 6th, 9th and 12th month. The primary efficacy endpoint of this study was the rate of change in thyroid nodule volume from baseline at 9 months of treatment. The rate of change in thyroid nodule volume from baseline at 3 and 6 months of treatment was a secondary efficacy endpoint. Other secondary efficacy endpoints included maximum thyroid nodule diameter, number of thyroid nodules, proportion of patients with reduced thyroid nodule volume or ≥50% from baseline, thyroid volume, thyroid function (serum TSH, FT3, FT4, thyroid egg levels (Tg), thyroid antibody levels (TgAb, TPOAb), quality of life evaluation (SF-36), etc. Safety endpoints included incidence of AE/ serious adverse events (SAE), causality, and outcomes. Incidence of AE/SAE leading to discontinuation. Changes in safety laboratory test values from baseline.

Interventions

• Drug regular dose of JiRui® Prunella oral liquid
  Take 10ml twice a day
• Drug 2x regular dose of JiRui® Prunella oral liquid
  Take 20ml twice a day
• Drug regular dose of placebo
  Take 10ml twice a day
• Drug 2x regular dose of placebo
  Take 20ml twice a day

Primary outcome measures

• Rate of change in thyroid nodule volume from baseline at 9 months of treatment. [Time frame: 270 ± 14 days]

Secondary outcome measures (12)

• Rate of change in thyroid nodule volume from baseline at 3 months of treatment. [Time frame: 90 ± 7 days.]
• Rate of change in thyroid nodule volume from baseline at 6 months of treatment. [Time frame: 180 ± 10 days.]
• Rate of change in thyroid nodule volume from baseline at 12 months of treatment. [Time frame: 360 ± 14 days.]
• The change value of the maximum diameter of thyroid nodules from baseline at 3 months of treatment. [Time frame: 90 ± 7 days]
• The change value of the maximum diameter of thyroid nodules from baseline at 6 months of treatment. [Time frame: 180 ± 10 days]
• The change value of the maximum diameter of thyroid nodules from baseline at 9 months of treatment. [Time frame: 270 ± 14 days]
• The change value of the maximum diameter of thyroid nodules from baseline at 12 months of treatment. [Time frame: 360 ± 14 days]
• Proportion of patients with reduced thyroid nodule volume from baseline at 3 months of treatment. [Time frame: 90 ± 7 days]
• Proportion of patients with reduced thyroid nodule volume from baseline at 6 months of treatment. [Time frame: 180 ± 10 days]
• Proportion of patients with reduced thyroid nodule volume from baseline at 9 months of treatment. [Time frame: 270 ± 14 days]
• Proportion of patients with reduced thyroid nodule volume from baseline at 12 months of treatment. [Time frame: 360 ± 14 days]
• Proportion of patients with reduced thyroid nodule volume ≥50% from baseline at 3 months of treatment. [Time frame: 90 ± 7 days]

Eligibility criteria

Inclusion criteria

• 18 years old ≤65 years old;
• Thyroid ultrasonography found thyroid nodules, may be accompanied by goiter, and the nodules meet the following conditions: 1) single nodules, or dominant nodules in multiple nodules (the largest diameter of the second largest nodules does not exceed 50% of the largest nodules), 2) solid nodules, 3) the longest diameter of nodules ≥1cm and < 3cm, 4) C-TIRADS 3\~4A nodules;
• Patients who met the puncture indications were confirmed by fine needle aspiration biopsy (FNAB) as benign nodules (Bethesda Class II);
• Serum TSH, free thyroid hormone (FT3, FT4) levels were normal, anti-thyroglobulin (TgAb) and anti-thyroid peroxidase (TPOAb) antibody titers were normal;
• Meet the diagnostic criteria of thyroid nodules in TCM;
• Sign the informed consent.

Exclusion criteria

• Exclude the patients with Deficiency of Yang syndrome, and the following two conditions can be diagnosed: Shortness of breath, abdominal pain and diarrhea, diarrhea with undigested food, Insufficiency with chills, exhaustion and lethargy, pale tongue and white fur, deep and weak pulse
• Those who have reproductive needs during pregnancy, lactation and within the last 12 months;
• Patients with high possibility of thyroid cancer indicated by ultrasonic signs and malignant confirmed by fine needle biopsy;
• Patients who meet the indications for thyroid nodule surgery, such as local compression symptoms obviously related to the nodule, the tumor is located behind the sternum or in the mediastinum, or strongly require surgery due to appearance or ideological concerns affecting normal life;
• Patients who have taken prunella preparations or other similar Chinese medicines to treat the disease within the past 1 month; Patients using glucocorticoids in the last 3 months;
• Patients who have had or plan to take thyroid hormone, iodine compound, or antithyroid drug therapy during the study period;
• Patients who have previously or plan to undergo ablation, neck radiation, surgery and other non-drug treatments during the study period;
• Patients with parathyroid tumor (PTA), medullary thyroid cancer (MTC) or other malignant tumors, or patients with serious cardiovascular disease, liver and kidney disease, osteoporosis, or patients with a history of mental illness;
• Patients with a family history of thyroid cancer or thyroid cancer syndrome;
• Laboratory test index ALT, AST > 1.5 times the upper limit of reference value or blood creatinine (Scr) > the upper limit of reference value;
• Persons who are known to be allergic to the investigational drug or its ingredients;
• Other patients determined by the investigator to be unsuitable for participation in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Double blind

Primary purpose

Treatment

Study locations

China · 22 centers

• Second Hospital of Army Military Medical University — Chongqing
• Xiamen Hospital of Traditional Chinese Medicine — Xiamen
• People's Hospital of Guangdong Province — Guangzhou
• Shenzhen Hospital of Peking University — Shenzhen
• Shunde Hospital of Southern Medical University — Shunde
• Wuhan First Hospital — Wuhan
• Jiangsu Province Hospital of Integrated Chinese and Western Medicine — Nanjing
• Xuzhou Medical University Hospital — Xuzhou
• … and 14 more centers

Identifiers

NCT: NCT06423235 · XK-22-A-002-YJ-002

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗