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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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07122232
Enrollment
177
Registered
2025-08-14
Start date
2023-04-01
Completion date
2023-09-30
Last updated
2025-08-14

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

Conditions

Malaria, Plasmodium Falciparum Infection, Plasmodium Vivax Infection, Thrombocytopenia

Keywords

Thrombocytopenia, Plasmodium falciparum, Malaria complications, Platelet count dynamics

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.

Interventions

None listed

Sponsors

Lady Reading Hospital, Pakistan
CollaboratorOTHER_GOV
Rafiullah Hotak
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age 18 years or older * Microscopically confirmed infection with Plasmodium vivax or Plasmodium falciparum * Provided written informed consen

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients with thrombocytopenia0 daysThe percentage of patients with platelet counts \<50×10³/µL at admission, compared between the P. vivax and P. falciparum groups.

Secondary

MeasureTime frameDescription
Platelet count recovery over timeDay 0 to Day 7Change in mean platelet count at admission, day 3, and day 7, for each group.

Other

MeasureTime frameDescription
Frequency of malaria-related complicationsWithin 7 days of admissionNumber of patients developing clinical complications (e.g., acute kidney injury, neurological involvement, anemia, jaundice), stratified by malaria species.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026