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Use of Mitomycin C to inhibit postoperative peridural fibrosis:a preliminary report

Use of Mitomycin C to inhibit postoperative peridural fibrosis:a preliminary report

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10001079
Enrollment
Unknown
Registered
2010-09-06
Start date
2010-03-15
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

lumbar intervertebral disc protrusion

Interventions

1:0.9%Sodium Chloride
2:0.5mg/ml Mitomycin C

Sponsors

The Affiliated Hospital With Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients presented with painful sciatica that was refractory to conservative treatment which had included bed rest, non-steroidal anti-inflammatory medication, epidural blocks and selective nerve root blocks and compression of the involved nerve root was confirmed by imaging studies.

Exclusion criteria

Exclusion criteria: 1. Patients were excluded if they had previously undergone spinal surgery, if they had been treated with epidural steroid drugs within 4 weeks of the proposed surgery, if they had been treated with oral steroid agents within 10 days of the surgery, or if they had received aspirin or other nonsteroidal antiinflammatory drugs within the 7 days preceding the surgery; 2. Patients who had undergone myelography or lumbar puncture within 24 hours of the surgery also wereexcluded. All patients were evaluated before the surgery by an internal medicine specialist who performed physical and cardiological examinations, chest radiographs, and standard laboratory analyses including complete blood count, chemistry panel, hepatic and renal tests, and urinalysis; 3. Patients with systemic illness, allergy, local/general infection,or slight anemia all were excluded from the study. To determine if there were any adverse effects of the drug, these same tests were done during the 1st week and the 1st month after surgery; no abnormality was found. Involvement in a workers’ compensation claim was another criterion for exclusion; 4. Patients were excluded intraoperatively if dural injury occurred.

Design outcomes

Primary

MeasureTime frame
The Image Score;

Secondary

MeasureTime frame
Physical Symptoms and Radiculopathy Score;Functional Disability and Activity-Related Pain;Leg Pain Severity Score;

Countries

China

Contacts

Public ContactXiaojian Cao
xiaojiancao@gmal.com+86 130025505801

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 2, 2026