Different Surgical Approaches in Patients of Early-stage Cervical Cancer
-
- STATUS
- Recruiting
-
- End date
- Nov 23, 2023
-
- participants needed
- 700
-
- sponsor
- Lei Li
Summary
This multi-center, randomized controlled study aims to compare the survival outcomes (including overall survival, progression-free survival and disease-free survival between Chinese uterine cervical patients receiving different surgical routes (laparotomy and laparoscopy) for radical hysterectomy or trachelectomy, which is the primary study objective. All patients with uterine cervical cancer of FIGO stage IA1 (with lymphovascular space invasion), IA2 and IB1 will be included and randomized into two groups: laparotomy and laparoscopy groups for radical hysterectomy or trachelectomy. Secondary study objectives include: patterns of recurrence, treatment-associated morbidity (6 months from surgery), cost-effectiveness, pelvic floor function, and quality of life.
Details
| Condition | Cervical Cancer, Cervical Cancer, Aspects of mortality statistics, Laparoscopy, Laparotomy, Disorders of cervix NOS, Uterine Cancer, Uterine Cancer, Morbidity, Survival, Mortality, Quality of life, Cost Effectiveness, Frequency, Pregnancy Complications, Pregnancy Complications, Pelvic Floor Disorders, quality-of-life, cervical neoplasm, diagnostic laparoscopy, laparoscopic procedures, laparoscopies |
|---|---|
| Treatment | Laparotomic radical hysterectomy, Laparoscopic radical hysterectomy, Laparotomic radical trachelectomy, Laparoscopic radical trachelectomy |
| Clinical Study Identifier | NCT03739944 |
| Sponsor | Lei Li |
| Last Modified on | 22 January 2021 |
Eligibility
How to participate?
,
You have contacted , on
Your message has been sent to the study team at ,
What happens next?
- You can expect the study team to contact you via email or phone in the next few days.
- Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.
You are contacting
Primary Contact
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
Learn moreSimilar trials to consider
Not finding what you're looking for?
Sign up as a volunteer to stay informed
Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.
Sign up as volunteer