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Scooped Curette for daily debridement and dressing

A Scopped Curette for Daily Wound Debridement and Dressing of Ulcers. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102111
Enrollment
50
Registered
2026-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: 8- Other Procedures Health Condition 2: 8- Other Procedures

Interventions

Intervention1: scooped curette used for daily wound debridement: Daily wound debridement was performed using a scooped curette under aseptic precautions to remove devitalized tissue while preserving h

Sponsors

Saveetha medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 18 years and above. Patients with chronic non healing wounds of more than four weeks duration. Wounds requiring regular mechanical debridement as part of standard wound care. Wound etiologies including diabetic foot ulcers venous leg ulcers pressure ulcers post traumatic or post surgical wounds. Wound size within a manageable range suitable for bedside debridement. Patients who are willing to undergo daily wound debridement using a scooped curette. Patients who are able to comply with daily wound care and follow up. Patients who provide written informed consent.

Exclusion criteria

Exclusion criteria: Critical limb ischemia, uncontrolled infection or sepsis, bleeding disorders or anticoagulation, malignant wounds, exposed bone/tendon/vessels, stable dry gangrene, severe pain intolerance, poor general condition, immunocompromised state, pregnancy, and inability to comply with follow-up

Design outcomes

Primary

MeasureTime frame
Effectiveness of wound debridement Time to achieve a clean wound bed Change in wound sizeTimepoint: Percentage reduction in wound area assessed at 2, 4, and 6 weeks Time to complete wound bed granulation within 4 weeks Time to readiness for definitive closure (grafting/secondary healing) within 6 weeks Incidence of procedure-related complications (bleeding, infection, pain) monitored throughout the study period (up to 6 weeks)

Secondary

MeasureTime frame
Bleeding during debridement (minimal / moderate / significant). Pain during procedure, assessed using Visual Analog Scale (VAS). Ease of debridement, as perceived by the operating surgeon. Need for definitive wound coverage (SSG, flap, secondary closure). Complications, if any (infection, excessive bleeding).Timepoint: Baseline (Day 0) Wound size, wound bed characteristics (slough, necrosis, granulation). Daily assessment Post-debridement wound bed status Bleeding and pain during procedure Day 7 Percentage of granulation tissue Change in wound area Day 14 Clean wound bed status Readiness for definitive coverage End of intervention When wound becomes suitable for closure or grafting Final wound measurements

Countries

India

Contacts

Public ContactGuna Sahithi lebaka

Saveetha medical college and hospital

drrajeshs80@yahoo.com8072425914

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026