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A Time-Point Comparison of Bleeding, Hematoma, Pain, and Discomfort with or without Sandbag Compression after Bone Marrow Examination

Pain, Discomfort and Bleeding in Relation to Bleeding control method and time after Bone Marrow Examination among Hemato-oncology Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011846
Enrollment
220
Registered
2026-04-14
Start date
2023-01-10
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

None listed

Interventions

None listed

Sponsors

Gachon University Gil Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with cancer or suspected hematologic disorders who underwent bone marrow examination in the hematology ward during the study period 2. Adults aged 19 years or older 3. Patients without spinal disorders associated with low back pain 4. Patients with normal cognitive and communication abilities 5. Patients who understood the questionnaire and voluntarily agreed to participate in the study

Exclusion criteria

Exclusion criteria: 1. Patients classified as high risk due to severely low platelet counts 2. Patients who had already received analgesics that could potentially interfere with pain assessment 3. Patients with skin infection or deformity at the bone marrow examination site (iliac crest)

Design outcomes

Primary

MeasureTime frame
Bleeding amount and the presence of hematoma measured after bone marrow examination—

Secondary

MeasureTime frame
Pain scores and discomfort scores measured after bone marrow examination—

Countries

Korea, Republic of

Contacts

Public ContactNari Seo

Gachon University Gil Medical Center

wapleice@naver.com+82-32-460-9260

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Apr 23, 2026