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NCT Number: NCT06007586

Prevention and Treatment of CINV Caused by TC Regimen in Gynecological Malignant Tumor Patients

To determine the best method to prevent CINV caused by TC regimen in patients with gynecological malignant tumor.

Paclitaxel-carboplatin (TC) is the most widely used regimen for gynecologic malignancies, yet chemotherapy-induced nausea and vomiting (CINV) remain common and distressing. Optimal prophylaxis is uncertain. This trial evaluated whether adding the NK1 receptor antagonist aprepitant to standard two-drug prophylaxis (5-HT3 receptor antagonist plus dexamethasone) improves CINV control.

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Key information

About this study

The risk of vomiting caused by high-dose carboplatin is controversial, and there is currently no prevention of TC in patients with gynecological malignant tumors High-level evidence-based medical evidence for programme-induced CINV. Therefore, different guidelines recommend the best antiemetic regimen as well It's different. This study is intended to conduct a prospective, multicenter, randomized, double-blind, placebo-controlled, crossover study The designed Phase III clinical study provides important data and basis for clinical practice and guideline formulation.

In this prospective, multicenter, double-blind, placebo-controlled, crossover phase III trial, patients with gynecologic malignancies scheduled for at least two cycles of TC were randomly assigned to receive aprepitant or placebo with ondansetron and dexamethasone during cycle 1, crossing over to the alternate regimen in cycle 2. The primary endpoint was complete response (CR: no emesis, no significant nausea and no rescue therapy) in the delayed phase (24-168 hours). Secondary endpoints included CR in acute and overall phases, nausea severity, rescue medication use, adverse events, and patient satisfaction.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Eligibility criteria: histologically confirmed gynecologic malignancies (including newly diagnosed cases and recurrent cases without chemo- or radiotherapy within the past six months); age 20-75 years; ECOG performance status 0-2; scheduled to receive at least two cycles of paclitaxel (175 mg/m²) plus carboplatin (AUC 5-6) every 3 weeks; and adequate organ function (bilirubin and creatinine within normal range, ALT and AST < 2× upper limit of normal).

Exclusion criteria

included prior chemotherapy, radiotherapy, or targeted therapy for the current recurrence; known brain metastases or history of brain tumors; history of gastrointestinal malignancy or major gastrointestinal surgery (except polypectomy or appendectomy); incomplete bowel obstruction; vestibular dysfunction; massive ascites (unless drained); concomitant opioid use; or diabetes mellitus.

Treatment and study plan

Aprepitant Injection

Drug

Two antiemetic groups use placebo, dexamethasone and ondansetron. Three antiemetic groups use aprepitant, dexamethasone and ondansetron.

Other names: dexamethasone, ondansetron

Primary outcomes

  1. Complete response (CR) rate in the delayed period

    Time frame: 24 hours to 7days after chemotherapy (each cycle is 21 days)

    CR is defined as no emesis, no significant nausea (VAS ≤4, where 0 = none, 10= = most severe), and no use of rescue antiemetics.

Secondary outcomes

  1. CR rates in the acute phase (0-24 hours) and overall phase (0-7 days).

    Time frame: acute phase: within 24 hours after chemotherapy (each cycle is 21 days); overall phase: within 7 days after chemotherapy (each cycle is 21 days).

    CR rates in the acute phase (0-24 hours) and overall phase (0-7 days).

  2. the use of rescue antiemetic

    Time frame: within 7 days after chemotherapy (each cycle is 21 days).

    the use of rescue antiemetic (0-7 days)

  3. patient satisfaction

    Time frame: On day 7 and 14 of each cycle (each cycle is 21 days).

    patient satisfaction assessed with a 7-point Likert-type scale (1=Very dissatisfied; 2=dissatisfied; 3=Relatively dissatisfied; 4=quite satisfied; 5=somewhat satisfied; 6=Satisfied; 7=Very satisfied)

  4. AEs

    Time frame: within 7 days after chemotherapy (each cycle is 21 days).

    incidence of adverse events

  5. severity of nausea

    Time frame: within 7 days after chemotherapy (each cycle is 21 days).

    severity of nausea (VAS: 0 = none, 10 = most severe)

Sponsors and collaborators

Lead sponsor

Sichuan Cancer Hospital and Research Institute

Other

Collaborators

  • Medical High Level Talents Program
  • Peking Union Medical College Hospital Talent Cultivation Program
  • Qilu Pharmaceutical Co., Ltd.
  • the Norman Bethune's "Research Wing Promotion"-Supporting Research Projects

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled Clinical Study on Prevention and Treatment of CINV Induced by TC Regimen in Gynecological Malignant Tumors

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 23, 2023
Registry last updated
Dec 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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