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CompletedNCT04891848Updated May 19, 2021

Assessment of Inflammation in Primary Headaches

An observational study in Headache Disorders, sponsored by Kocaeli University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-05-19.

Sponsored by Kocaeli University · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
230
Ages
18 Years to 65 Years
Sex
All
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Study summary

Headache is the most common neurological complaint accounting for % 1 to % 4 in the emergency department (ED).Every year, nearly one million people with headache attacks have been consulted by healthcare professionals at the emergency room in the United States.The International Classification of Headache Disorders (ICHD) divided headaches into two main groups: primary headaches and secondary headaches. The vast majority of cases who presented with acute headache attack in ED had a diagnosis of primary headache disorders (tension- type headache, migraine, cluster- type headache, and other primary headaches). However, secondary headache is often associated with underlying intracranial pathologies, and noted in % 10 of cases in emergency rooms. Despite the frequent presence of primary headaches, limited time setting and busy periods of medical assessment, leading diagnostic and therapeutic options due to the pathophysiological factors to be overlooked.

To date, no study in the emergency care setting has explored the role of inflammation in patients with acute migraine and TTH. Investigators aimed to explore inflammatory markers [white blood cells (WBC), neutrophil, lymphocyte, platelet, neutrophil / lymphocyte ratio (NLR), and platelet / lymphocyte ratio (PLR)] in complete blood count (CBC) among MA, MO, and TTH participants who admitted to ED with acute headache attack and healthy volunteers.

Read the detailed description

Study design This prospective study was completed at an emergency care of a tertiary referral hospital between May 2018 and May 2019. The hospital admits a total of 45.000 adult emergency patients per year. This study was approved by the local ethics Committee of Kocaeli University (KOU/KAE: 2018/192) in accordance with the Helsinki Declaration. Written and informed consent form was obtained from all individual participants.

Study population Investigators screened 720 patients who admitted to the ED with an acute headache attack. Clinical evaluation was performed by an experienced neurologist. Consequently, 51 patients with MA, 51 patients with MO, and 48 patients with TTH according to the diagnostic criterias of ICHD-3 and 80 age- and gender matched healthy controls were enrolled in this study. Detailed sociodemographic and clinical data collected using face-to-face interview. Visual analog scale (VAS) documented to measure the intensity of pain in patient groups.

Investigators included adult participants aged between 18 and 65 years. Also, subjects were eligible for inclusion if their body mass index (BMI) ranges were between18 kg/m2 and 30 kg/m2. Patients with secondary headaches, trauma, malignancy, chronic inflammatory disorders, infectious diseases, hematologic abnormalities, a prior history of surgery (within the preceding 6 months), receiving analgesics, antibiotics, blood transfusion and other blood products, were excluded from the study.

Laboratory analysis Complete blood count (CBC) parameters [WBC, neutrophil, lymphocyte, platelet] of patients and control groups were obtained from 2 cc peripheral venous blood samples (purple K3 EDTA tubes, Beckman Coulter DXH 800 Analyzer) during admission. NLR and PLR were calculated by dividing absolute neutrophil to absolute lymphocyte count and absolute platelet to absolute lymphocyte count, respectively.

Statistical Analysis SPSS 17.0 statistical software package program (IBM Corporation, USA) was used for the analysis. Descriptive data were presented using numbers, percentages (%) , mean ± standard deviation. Categorical variables were analyzed by using chi-square (χ2) test. Normality tests (Shapiro-Wilks, Lilliefors, and Kolmogorov-Smirnov) were used for all parameters. Due to the non-normal distribution of CBC values, Kruskal-Wallis and Tamhane's T2 post hoc tests were used to compare between patients with MA, MO, TTH, and healthy controls. A p value ≤ 0.05 considered statistically significant.

02

Conditions studied

  • Headache Disorders

Keywords

  • primary headache
  • migraine with aura
  • migraine without aura
  • tension type headache
  • inflammation
  • neuroinflammation
03

In context

Tension-Type Headache

144 studies on the registry are indexed under Tension-Type Headache; 41 are open to participants now.

This study's enrollment of 230 is above the median of 130 across 30 observational studies indexed under Tension-Type Headache.

Browse Tension-Type Headache studies →

Lead sponsor

Kocaeli University is the lead sponsor of 210 studies on the registry; 38 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Migraine and tension-type headache patients who admitted to emergency department with an acute headache attack

Inclusion criteria

  • Clinical diagnosis of Migraine
  • Clinical diagnosis of Tension- type headache
  • Age between 18 and 65 years
  • Body mass index between 18 kg/m2 and 30 kg/m2

Exclusion criteria

Exclusion Criteria;

  • Secondary headaches
  • Chronic inflammatory disorders
  • Infectious diseases
  • Hematologic abnormalities
  • A prior history of surgery (within the preceding 6 months)
  • Receiving analgesics
  • Blood transfusion before admission
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
230 participants (actual)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • migraine with aura

    51 patients with MA

    Other: inflammation

  • migraine without aura

    51 patients with migraine without aura

    Other: inflammation

  • tension type headache

    48 patients with tension type headache

    Other: inflammation

  • healthy controls

    80 healthy participants

    Other: inflammation

Interventions

  • Otherinflammation

    inflammatory values in complete blood count (CBC)

06

What researchers measure

Primary outcomes

  1. White blood cells

    White blood cells (x10³/μL) counted in complete blood count and compared between patients and healthy controls

    Time frame: Up to 1 year

  2. Neutrophil

    Neutrophil (x10³/μL) levels counted in complete blood count and compared between patients and healthy controls

    Time frame: Up to 1 year

  3. Lymphocyte

    Lymphocyte (x10³/μL) levels counted in complete blood count and compared between patients and healthy controls

    Time frame: Up to 1 year

  4. Platelet

    Platelet (x10³/μL) levels counted in complete blood count and compared between patients and healthy controls

    Time frame: Up to 1 year

  5. Neutrophil/lymphocyte ratio

    Neutrophil/lymphocyte ratio calculated by dividing absolute neutrophil to absolute lymphocyte and compared between patients and healthy controls.

    Time frame: Up to 1 year

  6. Platelet/lymphocyte ratio

    Platelet/lymphocyte ratio calculated by dividing absolute platelet to absolute lymphocyte and compared between patients and healthy controls.

    Time frame: Up to 1 year

07

Study locations

1 site
  • Halil Okay Albayrak
    Kocaeli, İzmit 41100, Turkey
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References and documents

Publications

  • Albayrak HO, Gurbuz H, Basaran S, Yilmaz S. Assessment of inflammation with hematological parameters in patients with migraine and tension-type headache: a prospective study from a tertiary care center. Pain Manag. 2022 Mar;12(2):141-148. doi: 10.2217/pmt-2021-0036. Epub 2021 Aug 25. PubMed 34431322 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 19, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04891848
Lead sponsor
Kocaeli University
Responsible party
Halil Okay Albayrak (Principal Investigator, Department of Emergency Medicine, Kocaeli University) — Principal investigator
First posted
May 19, 2021
Start date
May 1, 2018
Primary completion
May 31, 2019
Completion
May 31, 2019
Last update
May 19, 2021

Study contacts

Serkan Yılmaz, Prof
study chair · Kocaeli University Department of Emergency Medicine
Serkan Yılmaz, Prof
study director · Kocaeli University Department of Emergency Medicine

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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