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Trial · NCT07909590

A Study Evaluating the Impact of a Painkiller Product on Quality-of-Life and Daily Functioning

NCT07909590, Not yet recruiting, HALEON

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study Evaluating the Impact of a Painkiller Product on Quality-of-Life and Daily Functioning. Trials, record NCT07909590. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07909590

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Study Evaluating the Impact of a Painkiller Product on Quality-of-Life and Daily Functioning
NCT number
NCT07909590
Status
Not yet recruiting
Enrollment
2,100 participants, estimated
Lead sponsor
HALEON
Conditions
Pain
Interventions
Paracetamol
First posted
2026-11-02
Last updated
2026-11-02

Source ClinicalTrials.gov

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPain Intensity Before Using Panadol/DolexWithin the past 1 month from time of participation
Thinking about most recent headache episode, participants will be asked to rate the pain intensity experienced before using Panadol/Dolex on a scale 0 to 10, where 0= No pain and 10= Worst possible pain. Lower score indicates better outcome.
PrimaryPerceived Relief From Panadol/Dolex UseWithin the past 1 month from time of participationThinking about the headache episode, participants will describe the first sign of symptom relief they perceived after taking Panadol/Dolex.
PrimaryQoL Assessment After Using Panadol/Dolex Post Headache EpisodeWithin the past 1 month from time of participation
Thinking about most recent headache episode, participants will be asked to respond to 10 questions related to aspects of daily life when they used Panadol/Dolex after headache episode. The response will be scored using a 5-point scale, where 1= Not at all, and 5= Very Much. Lower score indicates better quality of life.
SecondaryFrequency of Panadol/Dolex UseWithin the past 1 month from time of participationThinking about the recent headache episode, participants will be asked to mention the frequency of product use from 1 time a day to 4 times a day.
SecondaryTimepoint of Panadol/Dolex UseWithin the past 1 month from time of participation
Participants will answer a single question related to timepoint of product use- 'Thinking about the same headache episode which you used Panadol for relief in the past one month, what did you first do to relieve the pain?' Participants will choose one of the given options.
SecondaryProduct SatisfactionWithin the past 1 month from time of participationThinking about the experience of using Panadol, participants will rate their overall satisfaction on a scale 1 to 5, where 1= Absolutely dissatisfied and 5= Completely satisfied.
SecondaryHeadache Management BehaviorsWithin the past 1 month from time of participation
Participants will answer a single question related to headache management approaches they used before- 'Thinking about similar headaches you experienced before this episode, what did you do to relieve your headache in the past?' Participants will select one or more descriptive options provided.
SecondaryUser Attitudes Towards Panadol/Dolex: Trust in The ProductWithin the past 1 month from time of participationParticipants will answer a single question related to trust in the product- 'How much do you trust the product to provide fast headache pain relief?' Participants will choose one of the given options.
SecondaryUser Attitudes Towards Panadol/Dolex: Value For MoneyWithin the past 1 month from time of participationThinking about experience of using the product, participants will be asked to rate the product's value for money on a scale 1 to 5, where 1= Poor value for money and 5= Excellent value for money.
SecondaryUser Attitudes Towards Panadol/Dolex: Intention to Use AgainWithin the past 1 month from time of participation
Participants will answer a single question related to continued purchase- 'How likely would you choose Panadol again for your next headache episode?'. Participants will choose one of the given options.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07909590

GET https://conductscience.org/api/trials/v1/NCT07909590/registered