Recruiting NA Cervical Cancer

New treatment option for Cervical Cancer

Official title Laparoscopic or Abdominal Radical Hysterectomy for Cervical Cancer(Stage IB1,IB2,IIA1)

ClinicalTrials.gov ID: NCT04929769

What this study is testing

What it's testing
The purpose of this study is to confirm whether there is a difference between laparoscopic radical hysterectomy (LRH) and abdominal radical hysterectomy (ARH) in patient survival for Cervical Cancer (Stage IB1, IB2, IIA1).
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 21 to 70, women only

You may be able to join if

  • Clinical diagnosis of squamous carcinoma of the cervix, adenocarcinoma, squamous adenocarcinoma (Stage IB1,IB2,IIA1).
  • Age ≥ 21 years and ≤ 70 years.
  • Surgery type B and C (refer to Q-M surgical staging)
  • Normal range of liver and kidney function and blood count (specific details below) Hemoglobin \> 60g/L Platelets \> 70\ 109/L Leukocytes \> 3\ 109/L...
  • No history of other malignancies.

You likely can't join if

  • Those who are contraindicated for various surgeries and cannot undergo surgery.
  • Patients who have received pelvic/abdominal radiotherapy irradiation or neoadjuvant chemotherapy for cervical cancer.
  • Patients with recurrent cervical cancer
  • Patients with CT, MRI or PET-CT suggesting suspicious metastasis of pelvic lymph nodes with maximum diameter \>2cm after further improvement of...
See the full eligibility criteria
Who can join
  • Clinical diagnosis of squamous carcinoma of the cervix, adenocarcinoma, squamous adenocarcinoma (Stage IB1,IB2,IIA1).
  • Age ≥ 21 years and ≤ 70 years.
  • Surgery type B and C (refer to Q-M surgical staging)
  • Normal range of liver and kidney function and blood count (specific details below) Hemoglobin \> 60g/L Platelets \> 70\ 109/L Leukocytes \> 3\ 109/L Creatinine \< 50mg/dL Transaminase abnormal indicators ≤ 3 Maximum...
  • No history of other malignancies.
  • Non-pregnancy.
  • Physical strength classification: Karnofsky score ≥ 60;
  • people voluntarily joined the study, signed the informed consent form, were compliant and cooperated with the follow-up.
  • No psychiatric disorders and other serious immune system disorders (e.g. lupus erythematosus, myasthenia gravis, HIV infection, etc.) (Note: Maximum diameter measurement of cervical lesions is based on PET-CT, or CT, or...
What rules you out
  • Those who are contraindicated for various surgeries and cannot undergo surgery.
  • Patients who have received pelvic/abdominal radiotherapy irradiation or neoadjuvant chemotherapy for cervical cancer.
  • Patients with recurrent cervical cancer
  • Patients with CT, MRI or PET-CT suggesting suspicious metastasis of pelvic lymph nodes with maximum diameter \>2cm after further improvement of preoperative examination.

The study team makes the final eligibility decision.

Where it's taking place

  • Shanghai, Shanghai Municipality, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling female, 21 years to 70 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Shanghai, Shanghai Municipality, China. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.