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Difference in serum creatinine level in cervical cancer patients treated with concurrent chemoradiation: Intravenous versus oral post-hydration: A randomized controlled trial

Difference in serum creatinine level in cervical cancer patients treated with concurrent chemoradiation: Intravenous versus oral post-hydration: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250920001
Enrollment
30
Registered
2025-09-20
Start date
2016-01-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

cervical cancer stage II-IV Cervical Neoplasms / drug therapy Cisplatin / adverse effects Hydration Therapy / methods Creatinine / blood

Interventions

After chemotherapy, this group received an additional 1000 mL of NSS with 10 mEq KCl intravenously over a two-hour period.,After chemotherapy, this group was instructed to consume 1000 mL of drinking
IV Hydration,Oral Hydration

Sponsors

Songklanagarind Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Newly diagnosed patients with pathologically proven Squamous cell carcinoma or Adenocarcinoma, classified as Stage II or III according to the International Federation of Gynecology and Obstetrics (FIGO) staging system, without obstructive uropathy, and who are being treated with concurrent chemoradiotherapy. 2.Patients have an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 2.

Exclusion criteria

Exclusion criteria: 1. The patient declined to continue/follow up with the treatment. 2. Female patients with a pre-treatment serum creatinine level greater than or equal to 1.2 mg/dL. 3. Patients with abnormal vital signs before, during, or after receiving medication, such as: Low blood pressure (hypotension) below 90/60 mmHg. Rapid heart rate (tachycardia) faster than 100 beats per minute. Rapid breathing (tachypnea) faster than 25 breaths per minute. Fever (elevated body temperature) higher than 38 C. 4. Patients with a history of underlying diseases, including heart, kidney, or liver disease/dysfunction.

Design outcomes

Primary

MeasureTime frame
serum creatinine 48 hour mg%

Secondary

MeasureTime frame
Electrolyte Abnormalities 48 hr potassium, magnesium levels,Hematologic Toxicities 48 hr white blood cell count, platelet count, anemia

Countries

Thailand

Contacts

Public ContactRakchai Buhachat

Prince of Songkhla University

brakchai@yahoo.com816783699

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026