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Observational study on the patients pain after undergoing bone marrow aspiration and biopsy

Exploring pain assessment and management needs of patients undergoing bone marrow aspiration and biopsy procedure - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/01/060986
Enrollment
93
Registered
2024-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Sharada Mailankody
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients undergoing bone marrow aspiration or biopsy procedure in the oncology departments

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain experienced by the patient as per numerical analog scaleTimepoint: Immediately after bone marrow procedure—

Secondary

MeasureTime frame
Factors associated with painTimepoint: After the procedure—

Countries

India

Contacts

Public ContactSharada Mailankody

Kasturba Medical College, Manipal

sharadajayaram27@gmail.com08202922779

Outcome results

None listed

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