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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05779111
Other study ID # CQGOG0111
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 10, 2022
Est. completion date December 10, 2022

Study information

Verified date February 2023
Source Chongqing University Cancer Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In previous studies, the investigators found that five factors were effective in predicting the probability of locally advanced cervical cancer with para-aortic lymph node metastasis.A retrospective study was conducted to explore the influence of 5 factors on PFS in patients with locally advanced cervical cancer receiving radiotherapy and chemotherapy.


Description:

In previous studies, the investigators found that five factors were effective in predicting the probability of locally advanced cervical cancer with para-aortic lymph node metastasis.5 factors included positive iliac lymph nodes, histological type, tumor size, positive pelvic lymph nodes on both sides, and maximum lymph node diameter greater than 1cm. Different factors give different scores.If the score is higher than 3, the probability of retroperitoneal lymph node metastasis in patients with locally advanced cervical cancer is significantly increased, and the prognosis of patients is affected. Patients with locally advanced cervix receiving radical radiotherapy were scored based on 5 factors.Patients with scores greater than or equal to 3 points were compared with patients with scores less than 3 points.


Recruitment information / eligibility

Status Completed
Enrollment 183
Est. completion date December 10, 2022
Est. primary completion date November 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Locally advanced cervical cancer patients receiving radiotherapy

Study Design


Locations

Country Name City State
China Chongqing Cancer Hospital Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Chongqing University Cancer Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression Free Survival(PFS) Whether there are differences in PFS between the two groups 3 months
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