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Fresh Frozen Plasma Transfusion in Acute Organophosphate Poisoning

A

Ain Shams University

Status

Enrolling

Conditions

Organophosphorus Poisoning

Treatments

Other: fresh frozen plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT06256796
plasma in OP poisoning

Details and patient eligibility

About

this study clinical trial to assess the role of fresh frozen plasma as a novel available and easy to be applied rather than conventional therapy on organophosphate poisoned patients and prediction of it is prognosis on selected patients and it is effect on outcome .

Full description

a prospective randomized clinical trail study . this study will be conducted in poison control center Ain shas university hospital -Egypt . all adult patients of both sexes admitted , in Poison Control Center of Ain Shams University Hospitals (PCC-ASUH) with diagnosis of moderate and severe degree of organophosphate poisoning will be included in this study.

The severity of patients under the study will be assessed at the time of presentation using the PeradeniyaOrganophosphorus Poisoning (POP) scale The severity will be graded as mild(0-3), moderate (4-7), and sever (8- 11).

The included patients in this study will be randomly divided into two groups as follow:

Group A: Patients who will be treated according to traditional management protocol of OPC toxicity in the form of: supportive measures, decontamination and antidotal therapy (atropine &Oximes) as follow:

  • Supportive measures and patients resuscitation.
  • Decontamination: patients presenting within 4hr of OP ingestion will be subjected to gastric lavage and all patients with oral exposure will be given a single (30 mg) dose of activated charcoal. Any contaminated material will be discarded and dermal contamination will be carried out using soap and water,if necessary.
  • Antidotal therapy: Atropine(each ampoule contains 1mg of atropine per ml) will be given as bolus doses of 2-5 mg IV and repeated every10-15 min until dryness of chest secretions, and then atropine injections maintenance doses will be given intermittently to patients as needed .Toxogonin (each ampoule contains 250mg of obidoxime chloride in 1 ml, produced by Merck, Darmstadt, Germany)will be administered as a loading dose of 250 mg, and will be repeated every 8 hrs until at least 12hrs after atropine no longer required.

This group of patients will be divided in to :

GroupA1 will include moderate degree of acute OP poisoned patients (POP scale 4-7) Group A2 will include severe degree of acute OP poisoned patients (POP scale 8-11)

Group B: Patients who will be treated with conventional therapy of OPC toxicity in the form of: supportive measures, decontamination and antidotal therapy (atropine &Oximes) in addition to fresh frozen plasma (FFP).

FFP will be given after one hour of hospitalization (time needed to prepare FFP to the patients and to finish emergency management) in dose of 20ml\kg given as follows:

  • 4 units first day
  • 3 units on second day 2 units on third day (

Enrollment

92 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-moderate and severe degree of organophosphate poisoning will be included in this study.

Exclusion criteria

  • patients below 18 years or above 60 years.
  • Patients with history of diabetes, cardiac disease, respiratory, renal disease and hepatic disease.
  • Pregnant female
  • Patients suspected of having mixed or unknown exposure
  • Patients with coagulation disorders.
  • Patients with hyper sensitivity to FFP or plasma derived products, as these cases are contraindicated to take fresh frozen plasma

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

92 participants in 4 patient groups

moderate group controlled patients
No Intervention group
moderate group study patients
Experimental group
Treatment:
Other: fresh frozen plasma
sever controlled group
No Intervention group
sever study group
Experimental group
Treatment:
Other: fresh frozen plasma

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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