Skip to content

"Assessing the effect of applying local cold and hot pack on the bruising extent of Enoxaparin sodium injection site in patients admitted "

Assessing the effect of applying local cold and hot pack on the bruising extent of Enoxaparin sodium injection site in patients admitted

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180623040206N1
Enrollment
74
Registered
2018-07-17
Start date
2018-07-10
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Diseases of skin and subcutaneouse tissue. L00-L99

Interventions

Intervention 1: Intervention group1: Samples(n=37) will receive per-filled syringe of enoxaparin sodium 6000 IU (prepared by Alborzdarou company), subcutaneously after administration on the right of

Sponsors

Research and Technology Deputy of Guilan University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: requiring hospital admission for at least 72 hours after receiving the second injection in the left abdomen treatment with Enoxaparin sodium with a dose of 6000 units having the results of the latest coagulation tests include INR, PTT, PT in the range of therapy (up to 1.5-2.5 as normal), normal amounts of platelets and hematocrit adequate renal function (creatinine 1.5-0.5 mg / dL) lack of extensive skin lesions on the abdomen such as extensive scarring due to surgery or burn lack of conditions preventing the correct implementation of the Enoxaparin injection method such as sever Ascites abdominal bruises from the previous injection satisfaction to participate in the research by signing a written consent

Exclusion criteria

Exclusion criteria: event of any change in the clinical condition is required changing in the amount or discontinuation of the drug performing subcutaneous injections Enoxaparin sodium on the right side of the abdomen by personnel unwillingness to continue cooperation

Design outcomes

Primary

MeasureTime frame
The extent of bruising in area of Enoxaparin sodium in Milimeter. Timepoint: 24,48 and 72 hours after intervention. Method of measurement: Recording the bruising extent based on multiplication of the largest diameter in the smallest diameter (by flexible ruler in millimeter) in prepared form.;The incidence of bruising in site of Enoxaparin sodium injection:discoloration in skin to violet color at least 2 mm. Timepoint: 24,48 and 72 hours after intervention. Method of measurement: Recording the observed bruising in prepared form by flexible ruler in millimeter)to measure skin discoloration.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtaollah asadi louyeh

Guilan university of medical sciences,Beheshti nursing and midwifery college

aa.louyeh@gums.ac.ir+98 13 3355 5056

Outcome results

None listed

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