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Efficacy and safety of lidocaine hydrochloride jelly for extubation of thoracic drainage tube after thoracic surgery.

Efficacy and safety of lidocaine hydrochloride jelly for extubation of thoracic drainage tube after thoracic surgery. - Efficacy and safety of lidocaine hydrochloride jelly for extubation of thoracic drainage tube.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013824
Enrollment
60
Registered
2014-04-30
Start date
2014-04-07
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients with chest tube after lung cancer radical operation.

Interventions

Lidocaine hydrochloride jelly 20mg/1ml Lidocaine hydrochloride cream 70mg/1ml Pracebo (sterilized jelly)

Sponsors

Department of Chest, Breast and Endocrinologic Surgery, Akita University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Shall meet the followin: 1) The case has been received a lung cancer radical operation and patients between 20 to 79 years of age. 2) The outstanding cases of enforced chemoradiationtherapy for lung cancer. 3) Performance Status (ECOG) of 0-1, and The American Society of Anesthesiologists physical status 0-1. 4) The outstanding cases of diabetes. 5) has the following organ function, adequate bone marrow, liver and renal function patients are kept White blood cell count >and= 3,000 / mm3 Neutrophil count >and= 1,500 / mm3 Platelet count >and= 100,000 / mm3 hemoglobin >and= 9.5g/dL AST / ALT; Less than 2.5 times the upper limit of normal facility Total Bilirubin <and= 1.5mg / dL Serum creatinene; more than 1.5 times the upper limit of normal SpO2 (Room air) 90% (PaO2 65mmHg or more) Less than 1+ proteinuira 6) At the time of the start date of administration, the patient has the following period has elapsed from prior treatment (1) radiation therapy For non-radiation to the chest: Longer than two weeks from the date of last exposure (2)surgical procedure (including pleurodesis) Without surgery lobectomy (include thoracotomy) 4 or more weeks Finish treatment (pleurodesis) more than two weeks 7) received a description of the contents of this trial, patient consent was obtained from the documents themselves

Exclusion criteria

Exclusion criteria: But if any one of the following will be excuded. 1) radiotherapy (radiation to the chest than excluded) 2) chemotherapy 3) patients with previously untreated brain metastasis 4) patients with infectious diseases and clinical problems 5) interstital pneumonia, pneumonitis, radiation pneumonitis, pulmonary infections, pulmonary fibrosis, patients have been complicated by pneumonia and other pulmonary disorder drug 6) clinical problems and complications (abnormal electrocardiogram, cardiac dysfunction, arrhythemias, and sever heart disease), patients with 7) patients with diabetes 8) patients with a large amount of ascites cardiac effusion pleural effusion 9) activity in patients with cancers 10) patients with a history of severe drug allergy 11) in patients who are pregnant or potentially pregnant lactating 12) In addition, patients were deemed unsuitable for the safe conduct of the study doctor

Design outcomes

Primary

MeasureTime frame
Wound pain and pain of extubation thoracic tube.

Countries

Japan

Contacts

Public ContactNobuyasu Kurihara

Akita University Graduate School of Medicine Department of Chest, Breast and Endocrinologic Surgery

kurihara@gipc.akita-u.ac.jp018-884-6132

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026