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Clinical Trials/ChiCTR2100043092
ChiCTR2100043092Active, not recruitingNot Applicable

疫检查点抑制剂治疗原发性肝癌诱发的肝损伤前瞻性登记研究

自筹1 site in 1 country200 target enrollmentStarted: February 1, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
肝功

Study Overview

Brief Summary

通过前瞻性登记研究,评估免疫检查点抑制剂治疗肝癌诱发的肝损伤的发病率、严重程度分布,探索肝损伤的危险因素,观察治疗的有效性,以提高该病的诊疗水平。

Study Design

Study Type
干预性研究
Primary Purpose
析因分组(即根据危险因素或暴露因素分组)
Masking
N/a

Eligibility Criteria

Ages
18 to 70 (—)
Sex
All

Inclusion Criteria

  • 影像学和 / 或病理学诊断为原发性肝细胞癌;
  • 应用免疫检查点抑制剂进行治疗;
  • 签署知情同意书。

Exclusion Criteria

  • 合并自身免疫性肝病;
  • 合并其它系统恶性肿瘤;
  • 无法配合完成随访者;
  • 肝损害重,CHILD 分级为 C 级者。

Arms & Interventions

根据肝损伤严重程度制定治疗方案

Outcomes

Primary Outcomes

肝功

Secondary Outcomes

  • 腹部 CT(每 3 月一次)

Investigators

Sponsor
自筹

Study Sites (1)

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