Comparative Study of Thrombocytopenia in Plasmodium Vivax and Falciparum Malaria
Comparative Analysis of Thrombocytopenia in Plasmodium Vivax and Plasmodium Falciparum Malaria: A Prospective Cross-Sectional Study From a Tertiary Care Hospital in Peshawar, Pakistan
1 other identifier
observational
177
1 country
1
Brief Summary
This study aimed to compare platelet count patterns in patients infected with either Plasmodium vivax or Plasmodium falciparum, the two most common malaria species in Pakistan. Thrombocytopenia (low platelet count) is a common complication of malaria and can help in identifying disease severity. We conducted this research at a tertiary care hospital in Peshawar, Pakistan, from April to September 2023. A total of 171 adult patients with confirmed malaria infections were enrolled. We measured their platelet counts at admission, day 3, and day 7, and analyzed the severity and progression of thrombocytopenia. The study found that while P. vivax was more common, P. falciparum was more likely to cause severe thrombocytopenia. Understanding these differences helps healthcare providers identify high-risk patients earlier and manage malaria more effectively. The study was approved by the institutional review board of Lady Reading Hospital, Peshawar.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2023
CompletedFirst Submitted
Initial submission to the registry
August 7, 2025
CompletedFirst Posted
Study publicly available on registry
August 14, 2025
CompletedAugust 14, 2025
August 1, 2025
6 months
August 7, 2025
August 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Proportion of patients with thrombocytopenia
The percentage of patients with platelet counts \<50×10³/µL at admission, compared between the P. vivax and P. falciparum groups.
0 days
Secondary Outcomes (1)
Platelet count recovery over time
Day 0 to Day 7
Other Outcomes (1)
Frequency of malaria-related complications
Within 7 days of admission
Study Arms (2)
Plasmodium vivax Group
Adult patients (≥18 years) with microscopically confirmed Plasmodium vivax malaria. Platelet counts and clinical data were collected at admission, day 3, and day 7 to assess the frequency and severity of thrombocytopenia.
Plasmodium falciparum Group
Adult patients (≥18 years) with microscopically confirmed Plasmodium falciparum malaria. Platelet counts and clinical data were collected at admission, day 3, and day 7 to assess the frequency and severity of thrombocytopenia.
Eligibility Criteria
Adult patients (aged 18 and above) presenting to a tertiary care hospital in Peshawar, Pakistan, with confirmed malaria infection. Participants were included based on microscopic confirmation of either Plasmodium vivax or Plasmodium falciparum infection and evaluated for platelet trends and clinical outcomes.
You may qualify if:
- Age 18 years or older
- Microscopically confirmed infection with Plasmodium vivax or Plasmodium falciparum
- Provided written informed consen
You may not qualify if:
- Mixed-species malaria infection
- Known hematologic disorders
- Chronic liver disease
- Recent blood transfusion
- Use of anticoagulant medication
- Incomplete parasitemia data or lost to follow-up
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Rafiullah Hotaklead
- Lady Reading Hospital, Pakistancollaborator
Study Sites (1)
Lady Reading Hospital, Medical Teaching Institution
Peshawar, KPK, 25000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rafiullah Hotak, MBBS
Nangarhar University faculty of medicine
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Student
Study Record Dates
First Submitted
August 7, 2025
First Posted
August 14, 2025
Study Start
April 1, 2023
Primary Completion
September 30, 2023
Study Completion
September 30, 2023
Last Updated
August 14, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share