ClinicalTrials.Veeva

Menu

A Comparative Study of Using Scorpion Antivenom Versus Scorpion Antivenom and Prazosin

S

Sohag University

Status and phase

Enrolling
Phase 4

Conditions

Morality

Treatments

Drug: Prazosin Oral Tablet

Study type

Interventional

Funder types

Other

Identifiers

NCT06287905
Soh-Med-23-02-24

Details and patient eligibility

About

Interventional study designed for the evaluation of characters and the outcome of scorpion sting patients will admit to Sohag University Hospitals in 2 randomized groups. The first group will receive scorpion antivenom only whether by the intravenous or the intramuscular route of administration. The second group will receive a combination of prazosin plus scorpion antivenom whether by the intravenous or the intramuscular route of administration. Both groups will receive proper first aid and supportive treatment

Full description

Tools of the study:

  1. Dose and administration of prazosin: 30 μg/kg/dose of prazosin will be delivered orally every 6 hours 4 doses, in adults we shouldn't exceed 1 mg per dose. Prazosin will be delivered using a nasogastric tube while securing the patient's airway in the event of vomiting or unconsciousness. Every 30 minutes for the first three hours, every hour for the following six, and then every four hours until improvement, blood pressure, pulse rate, respiration rate, and oxygen saturation will be measured. When pain is the only symptom, prophylaxis shouldn't be given. To avoid the first-dose phenomenon, the patient should remain in a laying position for around 3 hours (even while the case is being examined) (Shoreit et al., 2019).

    Dose of antivenom 1-1 ampoule intramuscular and/ or, 2-1 to 5 Polyvalent anti-scorpion serum ampoules produced by the vaccine & serum institution (VACSERA)in Egypt according to the severity of the case on 200 to 500 ml glucose 5% infusion and assess the patient clinically to repeat the dose after 4 to 6 hours. (Shoreit et al., 2019)

  2. A prepared sheet containing

    1. the demographic characteristics of each patient
    2. Vital signs and degree of coma at time of admission of the patient.
    3. First aid management as resuscitation.
    4. Supportive management will be done to the patients during the admission will be recorded.
    5. Cardiac enzymes measurements, duration of hospital stay and the outcome of patients in each group.

Enrollment

80 estimated patients

Sex

All

Ages

1 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • History and clinical diagnosis of scorpion sting
  • Admit in Sohag University hospitals
  • During the period from February 2023 to July 2024.
  • Accepting informed written consent from the case itself or the first degree relative if the case will underage or in a coma.

Exclusion criteria

  • .All other envenomation cases or poisoning will be excluded.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

80 participants in 2 patient groups

group of antivenom only
No Intervention group
Description:
Dose of antivenom 1-1 ampoule intramuscular and/ or, 2-1 to 5 Polyvalent anti-scorpion serum ampoules produced by the vaccine \& serum institution (VACSERA)in Egypt according to the severity of the case on 200 to 500 ml glucose 5% infusion and assess the patient clinically to repeat the dose after 4 to 6 hours. (Shoreit et al., 2019)
group of adding prazosin plus standard treatment
Experimental group
Description:
1-Dose and administration of prazosin: 30 μg/kg/dose of prazosin will be delivered orally every 6 hours 4 doses, in adults we shouldn't exceed 1 mg per dose. Prazosin will be delivered using a nasogastric tube while securing the patient's airway in the event of vomiting or unconsciousness. Every 30 minutes for the first three hours, every hour for the following six, and then every four hours until improvement, blood pressure, pulse rate, respiration rate, and oxygen saturation will be measured. When pain is the only symptom, prophylaxis shouldn't be given. To avoid the first-dose phenomenon, the patient should remain in a laying position for around 3 hours (even while the case is being examined) (Shoreit et al., 2019).
Treatment:
Drug: Prazosin Oral Tablet

Trial contacts and locations

1

Loading...

Central trial contact

Mai M Abd El Kader, PhD; Meray M Shokry Zaghary, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems