Updates are available Correction dated 2025-11-08

Article History

Received: 9 May 2025

Accepted: 15 September 2025

First Online: 14 October 2025

Change Date: 4 November 2025

Change Type: Update

Change Details: The original online version of this article was revised as two co-author names were inadvertently omitted from the list. This has been corrected now.

Change Date: 8 November 2025

Change Type: Correction

Change Details: A Correction to this paper has been published:

Change Details: https://doi.org/10.1007/s12070-025-06178-w

Declarations

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: The authors declare that they have no relevant affiliations or financial interests with any organization or entity that has a financial stake in, or a potential conflict of interest with, the subject matter or materials discussed in this manuscript. This includes, but is not limited to, employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents (received or pending), and royalties. All authors were actively involved in the conception, design, material preparation, and data collection for this study. The primary investigator specifically conducted the analysis and drafted the initial manuscript. All co-authors provided critical feedback on earlier versions and ultimately reviewed and approved the final manuscript for submission.

: Participants reviewed and understood the Patient Information Sheet prior to signing the Informed Consent Form. By signing, participants affirmed their consent to take part in the study titled “A randomised control trial to compare the use of autologous platelet rich plasma with conventional method in myringoplasty” to be conducted at the Tertiary Hospital. Key acknowledgements by participants include: The right to withdraw from the study at any time without justification and without affecting their medical care, understanding that their data and records will be kept confidential, acknowledgement that their data, if required, may be used for research purposes. The form includes spaces for the name and signature of the participant/patient, the investigator, and the date, time, and place. For illiterate participants or those unable to understand due to other reasons, spaces are provided for the name and signature of an impartial witness or legally acceptable relative, along with the date, time, and place.