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Dexamethasone Point Injection for Reducing Adverse Reaction of Chemotherapy: A Prospective Randomized Controlled Trial

Dexamethasone Point Injection for Reducing Adverse Reaction of Chemotherapy: A Prospective Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13004081
Enrollment
Unknown
Registered
2013-12-25
Start date
2014-02-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gynecological oncology

Interventions

treatment group:Acupoint injection of dexamethasone
control group:Acupoint injection of 0.9%NS

Sponsors

Changhai Hospital of Traditional Chinese Medicine, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) female, aged 18 to 70 years old; (2) diagnosed with gynecological tumors (ovarian, cervical, or endometrial cancer) based on pathology or cytology; (3) voluntary acceptance of the experimental treatment with informed consent, the informed consent process complied with GCP requirements; (4) Karnofsky scores higher than 60 points, with more than three months of expected survival and possible treatment with chemotherapy.

Exclusion criteria

Exclusion criteria: (1) diagnosis of functional damage to the liver, kidneys, or heart; (2) inability to follow the treatment because of regional mental abnormalities or pregnancy; (3) participating in other drug studies; (4) allergic constitution, has the history of drug allergy or known allergic to the medicine in the trial; (5) participation in other clinical trials in 3 months; (6) not sensitive or resistance th chemotherapy regimens; (7) using other drugs which could influence blood picture, anti-tumor or the immune function before starting the treatment; (8) the contraindications of dexamethasone: thrombosis, gastroduodenal ulcer, insanity and so on.

Design outcomes

Primary

MeasureTime frame
white blood cell count;

Secondary

MeasureTime frame
nausea and vomiting;treament costs;the dosage of granulocyte colony-stimulating factor;

Countries

China

Contacts

Public ContactYu Chaoqin

Shanghai Changhai Hospital

chqyu81@163.com+86 13818390984

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026