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A single-center, randomized, parallel-controlled clinical study comparing hydromorphone and morphine for perioperative analgesia in thyroid ablation surgery

A single-center, randomized, parallel-controlled clinical study comparing hydromorphone and morphine for perioperative analgesia in thyroid ablation surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123619
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Thyroid nodules and thyroid cancer

Interventions

Control Group (Group B):Intravenous Injection of Morphine Hydrochloride Injection
Experimental Group (Group A):Intravenous Injection of Hydromorphone Hydrochloride Injection

Sponsors

Bejing Tongren Hospital, Capital Medical Uniersity
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Voluntarily participate and sign the informed consent form in writing; 2.Aged 18 to 80, with no restriction on gender; 3.Patients scheduled for elective ablation surgery for thyroid nodules and thyroid cancer; 4.Eastern Cooperative Oncology Group (ECOG) Performance Status Score <= 2;

Exclusion criteria

Exclusion criteria: 1.Patients with severe coagulation disorders that cannot be corrected; 2.Patients with acute or severe bronchial asthma; 3.Patients with respiratory depression symptoms who lack cardiopulmonary resuscitation (CPR) equipment or monitoring devices; 4.Patients at risk of gastrointestinal obstruction, especially those with paralytic ileus; 5.Patients allergic to opioid drugs / patients with opioid addiction; 6.Abnormal laboratory results with significant clinical significance, such as serum creatinine = 2 times the upper limit of normal (ULN), alanine transaminase (ALT) or aspartate transaminase (AST) = 2.5 times the ULN, or Child-Pugh Class C liver function; 7.Patients with cognitive impairment; 8.Patients who used other analgesic drugs within 3 days before surgery; 9.Investigators directly involved in the trial or their family members; 10.Patients who participated in other clinical trials within the previous 30 days; 11.Other diseases and conditions that are considered ineligible for enrollment by the investigator;

Design outcomes

Primary

MeasureTime frame
Maximum Intraoperative Pain Score;Incidence of Adverse Reactions;

Secondary

MeasureTime frame
During the treatment period, monitor the patient's vital signs such as heart rate, blood pressure, blood oxygen saturation, and respiratory rate.;Duration of Surgery (min);Analgesic Drug Dosage (mg);Patient Satisfaction Assessment;NRS Scores at Each Measurement Time Point;Postoperative Recovery Quality Assessment (QoR-15);Concomitant Medications? / Rescue Medication Status / Rescue Medication Usage;Willingness to receive interventional treatment again after discharge;

Countries

China

Contacts

Public ContactWei Li

Bejing Tongren Hospital, Capital Medical Uniersity

vision988@126.com+86 10 84322470

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026