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NCT07504198Not yet recruitingPhase 2/3

Neuroprotection of Memantine and Rosuvastatin

Neuroprotective Effect of Memantine and Rosuvastatin Against Oxaliplatin Induced Peripheral Neuropathy in Patients With Colorectal Cancer

Source: ClinicalTrials.gov · Last updated 31 Mar 2026

Brief summary (registry, in English)

Memantine is used to slow the neurotoxicity of Alzheimer disease. Rosuvastatin used as a lipid-lowering agent . Increased bioavailability of endothelial-derived nitric oxide improves endothelium function , increases cerebral blood flow which may all contribute to the neuroprotective effects of rosuvastatin . The goal of this clinical trial is to prevent oxaliplatin induced peripheral neuropathy in patients with colorectal cancer.The aim of this current study is to assess the neuroprotective effect of memantine and rosuvastatin against oxaliplatin induced peripheral neuropathy.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
46 (estimated)
First submitted
15 Mar 2026
Start date
Mar 2026
Primary completion date
Apr 2027
Lead sponsor
Tanta University
NCT number
NCT07504198

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 46
  • From Mar 2026 to the primary completion date, Apr 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior exposure to neurotoxic chemotherapy (oxaliplatin, cisplatin, vincristine, paclitaxel, or docetaxel, INH).
  • Concomitant use of multivitamins (vitamins E, C, A), tricyclic antidepressants, other neuro-protective medications (gabapentin, lamotrigine, carbamazepine and phenytoin).
  • Concurrent active cancer originating from a primary site other than colon or rectum.

Other illness

  • Patients with diabetes and other conditions that predispose to neuropathy as hypothyroidism, autoimmune diseases, hepatitis C.
  • History of known allergy to oxaliplatin or other platinum agents.
  • Patients with other inflammatory or stressful conditions.

Lab values

  • Patients on amantadine , acetazolamide, dextromethorphan, aluminum hydroxide magnesium hydroxide and febuxostat .
  • Sever renal insufficiency (creatinine clearance \< 25 ml/ minute) .

Age

  • Children \< 18 years old.

Other

  • Pregnant and breastfeeding women.

Who the study is looking for

  • Age above 18 years old for both gender .
  • Adequate baseline hematologic values (absolute neutrophil count ≥ 1.5 × 109/L, platelet count ≥ 100 × 109/L and hemoglobin level ≥ 10 g/dl).
  • Patients with adequate renal function (serum creatinine \< 1.5 mg/dl or creatinine clearance ˃ 45 mL/min).
  • Patients with adequate liver function (serum bilirubin \< 1.5 mg/dl).
  • Patients with performance status \<2 according to Eastern Cooperative Oncology Group (ECOG) score.
  • Patients who will be scheduled to receive modified FOLFOX-6 or XELOX regimen.
  • Patients with histologically confirmed diagnosis of stage III or stage IV colorectal cancer.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tanta
Coordinator of this site? Confirm its status
TantaEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.